ENST00000304895.9:c.1828A=
MANE Select
|
ENSP00000302728.4:p.Thr610=
|
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ENST00000304895.8:c.1828A=
|
ENSP00000302728.4:p.Thr610=
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|
ENST00000421103.5:c.1390A=
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ENSP00000391390.1:p.Thr464=
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ENST00000430730.5:c.*1095A=
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ENSP00000411859.1:n.*1095A=
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ENST00000447929.5:c.*1208A=
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ENSP00000411262.1:n.*1208A=
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ENST00000466883.5:n.2218A=
|
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NM_000181.3:c.1828A=
|
NP_000172.2:p.Thr610=
|
|
NM_001284290.1:c.1390A=
|
NP_001271219.1:p.Thr464=
|
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NM_001293104.1:c.1258A=
|
NP_001280033.1:p.Thr420=
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NM_001293105.1:c.1171A=
|
NP_001280034.1:p.Thr391=
|
|
NR_120531.1:n.1874A=
|
|
|
XM_005250297.3:c.1675A=
|
XP_005250354.1:p.Thr559=
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|
XM_011516113.1:c.1327A=
|
XP_011514415.1:p.Thr443=
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|
XM_011516114.1:c.1156A=
|
XP_011514416.1:p.Thr386=
|
|
XM_005250297.4:c.1675A=
|
XP_005250354.1:p.Thr559=
|
|
XM_011516114.2:c.1156A=
|
XP_011514416.1:p.Thr386=
|
|
XM_017012091.1:c.1174A=
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XP_016867580.1:p.Thr392=
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|
XM_017012092.1:c.1105A=
|
XP_016867581.1:p.Thr369=
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|
XM_017012093.2:c.1003A=
|
XP_016867582.1:p.Thr335=
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XR_001744658.2:n.1635A=
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XR_001744659.2:n.1748A=
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XR_001744660.2:n.1680A=
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XR_001744661.2:n.1595A=
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XR_927461.3:n.1833A=
|
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|
NM_000181.4:c.1828A=
MANE Select
|
NP_000172.2:p.Thr610=
|
|
NM_001284290.2:c.1390A=
|
NP_001271219.1:p.Thr464=
|
|
NM_001293104.2:c.1258A=
|
NP_001280033.1:p.Thr420=
|
|
NM_001293105.2:c.1171A=
|
NP_001280034.1:p.Thr391=
|
|
NR_120531.2:n.1773A=
|
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