ENST00000216361.9:c.1052G>T
|
ENSP00000216361.5:p.Gly351Val
|
|
ENST00000396618.9:c.857G>T
MANE Select
|
ENSP00000379862.3:p.Gly286Val
|
|
ENST00000555117.2:c.914G>T
|
ENSP00000493569.1:p.Gly305Val
|
|
ENST00000643575.1:c.857G>T
|
ENSP00000494838.1:p.Gly286Val
|
|
ENST00000643697.1:n.1159G>T
|
|
|
ENST00000644874.2:c.857G>T
|
ENSP00000496360.1:p.Gly286Val
|
|
ENST00000216361.8:c.857G>T
|
ENSP00000216361.4:p.Gly286Val
|
|
ENST00000396618.7:c.857G>T
|
ENSP00000379862.3:p.Gly286Val
|
|
ENST00000460581.6:c.521G>T
|
ENSP00000451713.1:p.Gly174Val
|
|
ENST00000468826.2:c.508G>T
|
|
|
ENST00000475087.5:c.857G>T
|
ENSP00000451528.1:p.Gly286Val
|
|
ENST00000555881.5:c.503G>T
|
ENSP00000452569.1:p.Gly168Val
|
|
ENST00000557065.1:c.639G>T
|
ENSP00000451629.1:n.639G>T
|
|
NM_001135058.1:c.857G>T
|
NP_001128530.1:p.Gly286Val
|
|
NM_004086.2:c.857G>T
|
NP_004077.1:p.Gly286Val
|
|
NR_038356.1:n.1348C>A
|
|
|
XM_011536539.1:c.857G>T
|
XP_011534841.1:p.Gly286Val
|
|
NM_001347720.1:c.1052G>T
|
NP_001334649.1:p.Gly351Val
|
|
XM_017021071.1:c.1052G>T
|
XP_016876560.1:p.Gly351Val
|
|
XM_024449506.1:c.914G>T
|
XP_024305274.1:p.Gly305Val
|
|
NM_004086.3:c.857G>T
MANE Select
|
NP_004077.1:p.Gly286Val
|
|
NM_001135058.2:c.857G>T
|
NP_001128530.1:p.Gly286Val
|
|
NM_001347720.2:c.1052G>T
|
NP_001334649.1:p.Gly351Val
|
|