ENST00000265641.10:c.236C>A
MANE Select
|
ENSP00000265641.4:p.Pro79His
|
|
ENST00000265641.9:c.236C>A
|
ENSP00000265641.4:p.Pro79His
|
|
ENST00000376618.6:c.236C>A
|
ENSP00000365803.2:p.Pro79His
|
|
ENST00000539743.5:c.236C>A
|
ENSP00000446108.1:p.Pro79His
|
|
ENST00000540367.5:c.236C>A
|
ENSP00000439084.1:p.Pro79His
|
|
ENST00000561996.1:c.236C>A
|
ENSP00000457663.1:p.Pro79His
|
|
ENST00000565318.5:c.236C>A
|
ENSP00000457826.1:p.Pro79His
|
|
ENST00000569129.5:c.236C>A
|
ENSP00000455116.1:p.Pro79His
|
|
NM_001031847.2:c.236C>A
|
NP_001027017.1:p.Pro79His
|
|
NM_001876.3:c.236C>A
|
NP_001867.2:p.Pro79His
|
|
XM_005273762.1:c.332C>A
|
XP_005273819.1:p.Pro111His
|
|
XM_005273763.1:c.332C>A
|
XP_005273820.1:p.Pro111His
|
|
XM_005273762.3:c.332C>A
|
XP_005273819.1:p.Pro111His
|
|
XM_017017220.1:c.236C>A
|
XP_016872709.1:p.Pro79His
|
|
NM_001876.4:c.236C>A
MANE Select
|
NP_001867.2:p.Pro79His
|
|
NM_001031847.3:c.236C>A
|
NP_001027017.1:p.Pro79His
|
|