ENST00000272286.4:c.1913A>G
MANE Select
|
ENSP00000272286.2:p.Tyr638Cys
|
|
ENST00000272286.2:c.1913A>G
|
ENSP00000272286.2:p.Tyr638Cys
|
|
NM_022437.2:c.1913A>G
|
NP_071882.1:p.Tyr638Cys
|
|
XM_005264483.2:c.1910A>G
|
XP_005264540.1:p.Tyr637Cys
|
|
XM_011533029.1:c.1925A>G
|
XP_011531331.1:p.Tyr642Cys
|
|
XM_011533030.1:c.1922A>G
|
XP_011531332.1:p.Tyr641Cys
|
|
XM_011533031.1:c.1697A>G
|
XP_011531333.1:p.Tyr566Cys
|
|
XR_939707.1:n.2415A>G
|
|
|
NM_001357321.1:c.1910A>G
|
NP_001344250.1:p.Tyr637Cys
|
|
XM_011533029.2:c.1925A>G
|
XP_011531331.1:p.Tyr642Cys
|
|
XM_011533030.2:c.1922A>G
|
XP_011531332.1:p.Tyr641Cys
|
|
XR_001738891.1:n.2429A>G
|
|
|
XR_939707.2:n.2429A>G
|
|
|
NM_022437.3:c.1913A>G
MANE Select
|
NP_071882.1:p.Tyr638Cys
|
|
NM_001357321.2:c.1910A>G
|
NP_001344250.1:p.Tyr637Cys
|
|