ENST00000422737.7:c.4676G>T
|
ENSP00000415650.3:p.Gly1559Val
|
|
ENST00000457135.2:c.885G>T
|
|
|
ENST00000334344.11:c.4676G>T
MANE Select
|
ENSP00000335044.6:p.Gly1559Val
|
|
ENST00000422737.6:c.4597G>T
|
|
|
ENST00000334344.10:c.4676G>T
|
ENSP00000335044.6:p.Gly1559Val
|
|
ENST00000422737.5:c.4229G>T
|
ENSP00000415650.1:p.Gly1410Val
|
|
ENST00000444670.5:c.3506G>T
|
ENSP00000397307.1:p.Gly1169Val
|
|
ENST00000457135.1:c.500G>T
|
ENSP00000388357.1:p.Gly167Val
|
|
ENST00000479608.5:n.3967G>T
|
|
|
NM_152641.2:c.4676G>T
|
NP_689854.2:p.Gly1559Val
|
|
XM_006719272.2:c.4676G>T
|
XP_006719335.1:p.Gly1559Val
|
|
XM_011538025.1:c.3044G>T
|
XP_011536327.1:p.Gly1015Val
|
|
XR_944505.1:n.4824G>T
|
|
|
NM_001347839.1:c.4676G>T
|
NP_001334768.1:p.Gly1559Val
|
|
NM_152641.3:c.4676G>T
|
NP_689854.2:p.Gly1559Val
|
|
XM_006719272.4:c.4676G>T
|
XP_006719335.1:p.Gly1559Val
|
|
XR_944505.3:n.4807G>T
|
|
|
NM_152641.4:c.4676G>T
MANE Select
|
NP_689854.2:p.Gly1559Val
|
|
NM_001347839.2:c.4676G>T
|
NP_001334768.1:p.Gly1559Val
|
|