ENST00000700075.1:c.19G=
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ENSP00000514784.1:p.Ala7=
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ENST00000342771.10:c.1951G=
MANE Select
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ENSP00000344087.4:p.Ala651=
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ENST00000439256.2:c.49G=
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ENSP00000407058.2:p.Ala17=
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ENST00000443672.2:c.286G=
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ENSP00000393548.2:p.Ala96=
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ENST00000449547.6:c.44G=
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ENST00000464768.2:n.619G=
|
|
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ENST00000644359.1:c.532G=
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ENSP00000494561.1:p.Ala178=
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ENST00000644506.1:c.577G=
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ENSP00000496672.1:p.Ala193=
|
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ENST00000644939.1:c.1948G=
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ENSP00000496726.1:p.Ala650=
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ENST00000644949.1:c.282G=
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ENST00000646136.1:n.262G=
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|
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ENST00000647140.1:c.816G=
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ENST00000342771.8:c.1951G=
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ENSP00000344087.4:p.Ala651=
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ENST00000406775.6:c.1879G=
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ENSP00000385263.2:p.Ala627=
|
|
ENST00000439256.1:c.49G=
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|
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ENST00000443672.1:c.531G=
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|
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ENST00000464768.1:n.617G=
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ENST00000465899.1:n.448G=
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ENST00000498384.5:n.319G=
|
|
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ENST00000611706.4:c.1207G=
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ENSP00000478134.1:p.Ala403=
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ENST00000615871.4:c.1135G=
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ENSP00000479325.1:p.Ala379=
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NM_001127231.2:c.1879G=
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NP_001120703.1:p.Ala627=
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NM_015570.3:c.1951G=
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NP_056385.1:p.Ala651=
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XM_005250257.1:c.598G=
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XP_005250314.1:p.Ala200=
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XM_011516010.1:c.1972G=
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XP_011514312.1:p.Ala658=
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XM_011516011.1:c.1969G=
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XP_011514313.1:p.Ala657=
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XM_011516012.1:c.1906G=
|
XP_011514314.1:p.Ala636=
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XM_011516013.1:c.1900G=
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XP_011514315.1:p.Ala634=
|
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XM_011516014.1:c.1870G=
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XP_011514316.1:p.Ala624=
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XM_011516015.1:c.1708G=
|
XP_011514317.1:p.Ala570=
|
|
XM_011516016.1:c.1681G=
|
XP_011514318.1:p.Ala561=
|
|
XM_011516017.1:c.1498G=
|
XP_011514319.1:p.Ala500=
|
|
XM_011516018.1:c.1471G=
|
XP_011514320.1:p.Ala491=
|
|
XM_005250257.2:c.598G=
|
XP_005250314.1:p.Ala200=
|
|
XM_011516010.2:c.1972G=
|
XP_011514312.1:p.Ala658=
|
|
XM_011516011.2:c.1969G=
|
XP_011514313.1:p.Ala657=
|
|
XM_011516012.2:c.1906G=
|
XP_011514314.1:p.Ala636=
|
|
XM_011516013.2:c.1900G=
|
XP_011514315.1:p.Ala634=
|
|
XM_011516014.2:c.1870G=
|
XP_011514316.1:p.Ala624=
|
|
XM_011516017.2:c.1498G=
|
XP_011514319.1:p.Ala500=
|
|
XM_011516018.2:c.1471G=
|
XP_011514320.1:p.Ala491=
|
|
XM_017011951.2:c.1972G=
|
XP_016867440.1:p.Ala658=
|
|
NM_001127231.3:c.1879G=
|
NP_001120703.1:p.Ala627=
|
|
NM_015570.4:c.1951G=
MANE Select
|
NP_056385.1:p.Ala651=
|
|