ENST00000422737.7:c.4672G>T
|
ENSP00000415650.3:p.Ala1558Ser
|
|
ENST00000457135.2:c.881G>T
|
|
|
ENST00000334344.11:c.4672G>T
MANE Select
|
ENSP00000335044.6:p.Ala1558Ser
|
|
ENST00000422737.6:c.4593G>T
|
|
|
ENST00000334344.10:c.4672G>T
|
ENSP00000335044.6:p.Ala1558Ser
|
|
ENST00000422737.5:c.4225G>T
|
ENSP00000415650.1:p.Ala1409Ser
|
|
ENST00000444670.5:c.3502G>T
|
ENSP00000397307.1:p.Ala1168Ser
|
|
ENST00000457135.1:c.496G>T
|
ENSP00000388357.1:p.Ala166Ser
|
|
ENST00000479608.5:n.3963G>T
|
|
|
NM_152641.2:c.4672G>T
|
NP_689854.2:p.Ala1558Ser
|
|
XM_006719272.2:c.4672G>T
|
XP_006719335.1:p.Ala1558Ser
|
|
XM_011538025.1:c.3040G>T
|
XP_011536327.1:p.Ala1014Ser
|
|
XR_944505.1:n.4820G>T
|
|
|
NM_001347839.1:c.4672G>T
|
NP_001334768.1:p.Ala1558Ser
|
|
NM_152641.3:c.4672G>T
|
NP_689854.2:p.Ala1558Ser
|
|
XM_006719272.4:c.4672G>T
|
XP_006719335.1:p.Ala1558Ser
|
|
XR_944505.3:n.4803G>T
|
|
|
NM_152641.4:c.4672G>T
MANE Select
|
NP_689854.2:p.Ala1558Ser
|
|
NM_001347839.2:c.4672G>T
|
NP_001334768.1:p.Ala1558Ser
|
|