ENST00000336112.9:c.3950G>T
|
ENSP00000337250.5:p.Gly1317Val
|
|
ENST00000435504.9:c.3953G>T
MANE Select
|
ENSP00000391447.3:p.Gly1318Val
|
|
ENST00000336112.8:c.3869G>T
|
ENSP00000337250.4:p.Gly1290Val
|
|
ENST00000404843.5:c.2402G>T
|
ENSP00000383920.1:p.Gly801Val
|
|
ENST00000435504.8:c.3953G>T
|
ENSP00000391447.3:p.Gly1318Val
|
|
NM_018263.4:c.3953G>T
|
NP_060733.4:p.Gly1318Val
|
|
XM_006712039.2:c.3587G>T
|
XP_006712102.1:p.Gly1196Val
|
|
XM_006712040.1:c.3173G>T
|
XP_006712103.1:p.Gly1058Val
|
|
XM_011532950.1:c.3950G>T
|
XP_011531252.1:p.Gly1317Val
|
|
XM_011532951.1:c.3779G>T
|
XP_011531253.1:p.Gly1260Val
|
|
NM_018263.5:c.3953G>T
|
NP_060733.4:p.Gly1318Val
|
|
XM_006712039.3:c.3587G>T
|
XP_006712102.1:p.Gly1196Val
|
|
XM_006712040.2:c.3173G>T
|
XP_006712103.1:p.Gly1058Val
|
|
XM_011532950.3:c.3950G>T
|
XP_011531252.1:p.Gly1317Val
|
|
XM_011532951.2:c.3779G>T
|
XP_011531253.1:p.Gly1260Val
|
|
XM_017004430.1:c.3173G>T
|
XP_016859919.1:p.Gly1058Val
|
|
XM_024452974.1:c.4133G>T
|
XP_024308742.1:p.Gly1378Val
|
|
NM_001369346.1:c.3779G>T
|
NP_001356275.1:p.Gly1260Val
|
|
NM_001369347.1:c.3173G>T
|
NP_001356276.1:p.Gly1058Val
|
|
NM_018263.6:c.3953G>T
MANE Select
|
NP_060733.4:p.Gly1318Val
|
|