ENST00000356141.9:c.1897C>G
MANE Select
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ENSP00000348460.4:p.Pro633Ala
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ENST00000551634.6:c.1906C>G
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ENSP00000448373.2:p.Pro636Ala
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|
ENST00000680362.1:c.1797C>G
|
|
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ENST00000681323.1:c.793+2623C>G
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ENST00000346562.6:c.1801C>G
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ENSP00000319610.5:p.Pro601Ala
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ENST00000356141.8:c.1897C>G
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ENSP00000348460.4:p.Pro633Ala
|
|
ENST00000357798.9:c.1858C>G
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ENSP00000350446.5:p.Pro620Ala
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ENST00000548645.5:c.1807C>G
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ENSP00000448916.1:p.Pro603Ala
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ENST00000551492.5:c.1912C>G
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ENSP00000450392.1:p.Pro638Ala
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ENST00000551634.5:c.1819C>G
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ENSP00000448373.1:p.Pro607Ala
|
|
NM_001164749.1:c.1897C>G
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NP_001158221.1:p.Pro633Ala
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|
NM_001165893.1:c.1807C>G
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NP_001159365.1:p.Pro603Ala
|
|
NM_022123.2:c.1801C>G
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NP_071406.1:p.Pro601Ala
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NM_173159.2:c.1858C>G
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NP_775182.1:p.Pro620Ala
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|
XM_005267991.2:c.1918C>G
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XP_005268048.1:p.Pro640Ala
|
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XM_005267992.2:c.1912C>G
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XP_005268049.1:p.Pro638Ala
|
|
XM_005267993.2:c.1858C>G
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XP_005268050.1:p.Pro620Ala
|
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XM_011537067.1:c.1948C>G
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XP_011535369.1:p.Pro650Ala
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XM_011537068.1:c.1939C>G
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XP_011535370.1:p.Pro647Ala
|
|
XM_011537069.1:c.1909C>G
|
XP_011535371.1:p.Pro637Ala
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|
XM_011537070.1:c.1852C>G
|
XP_011535372.1:p.Pro618Ala
|
|
XM_011537071.1:c.1819C>G
|
XP_011535373.1:p.Pro607Ala
|
|
XM_011537072.1:c.1798C>G
|
XP_011535374.1:p.Pro600Ala
|
|
XM_011537073.1:c.1591C>G
|
XP_011535375.1:p.Pro531Ala
|
|
XM_011537074.1:c.1591C>G
|
XP_011535376.1:p.Pro531Ala
|
|
XM_005267991.3:c.2005C>G
|
XP_005268048.2:p.Pro669Ala
|
|
XM_005267992.3:c.1999C>G
|
XP_005268049.2:p.Pro667Ala
|
|
XM_011537067.2:c.1948C>G
|
XP_011535369.1:p.Pro650Ala
|
|
XM_011537069.2:c.1996C>G
|
XP_011535371.2:p.Pro666Ala
|
|
XM_011537070.2:c.1852C>G
|
XP_011535372.1:p.Pro618Ala
|
|
XM_011537071.2:c.1906C>G
|
XP_011535373.2:p.Pro636Ala
|
|
XM_011537072.2:c.1798C>G
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XP_011535374.1:p.Pro600Ala
|
|
XM_017021582.1:c.2056C>G
|
XP_016877071.1:p.Pro686Ala
|
|
XM_017021583.1:c.2047C>G
|
XP_016877072.1:p.Pro683Ala
|
|
XM_017021584.1:c.1966C>G
|
XP_016877073.1:p.Pro656Ala
|
|
XM_017021585.1:c.1915C>G
|
XP_016877074.1:p.Pro639Ala
|
|
XM_017021586.1:c.1591C>G
|
XP_016877075.1:p.Pro531Ala
|
|
XM_017021587.1:c.1591C>G
|
XP_016877076.1:p.Pro531Ala
|
|
XM_017021588.1:c.1591C>G
|
XP_016877077.1:p.Pro531Ala
|
|
NM_001164749.2:c.1897C>G
MANE Select
|
NP_001158221.1:p.Pro633Ala
|
|
NM_001165893.2:c.1807C>G
|
NP_001159365.1:p.Pro603Ala
|
|
NM_022123.3:c.1801C>G
|
NP_071406.1:p.Pro601Ala
|
|
NM_173159.3:c.1858C>G
|
NP_775182.1:p.Pro620Ala
|
|
NM_001394988.1:c.1852C>G
|
NP_001381917.1:p.Pro618Ala
|
|
NM_001394989.1:c.1798C>G
|
NP_001381918.1:p.Pro600Ala
|
|