ENST00000216361.9:c.1053C>G
|
ENSP00000216361.5:p.Gly351=
|
|
ENST00000396618.9:c.858C>G
MANE Select
|
ENSP00000379862.3:p.Gly286=
|
|
ENST00000555117.2:c.915C>G
|
ENSP00000493569.1:p.Gly305=
|
|
ENST00000643575.1:c.858C>G
|
ENSP00000494838.1:p.Gly286=
|
|
ENST00000643697.1:n.1160C>G
|
|
|
ENST00000644874.2:c.858C>G
|
ENSP00000496360.1:p.Gly286=
|
|
ENST00000216361.8:c.858C>G
|
ENSP00000216361.4:p.Gly286=
|
|
ENST00000396618.7:c.858C>G
|
ENSP00000379862.3:p.Gly286=
|
|
ENST00000460581.6:c.522C>G
|
ENSP00000451713.1:p.Gly174=
|
|
ENST00000468826.2:c.509C>G
|
|
|
ENST00000475087.5:c.858C>G
|
ENSP00000451528.1:p.Gly286=
|
|
ENST00000555881.5:c.504C>G
|
ENSP00000452569.1:p.Gly168=
|
|
ENST00000557065.1:c.640C>G
|
ENSP00000451629.1:n.640C>G
|
|
NM_001135058.1:c.858C>G
|
NP_001128530.1:p.Gly286=
|
|
NM_004086.2:c.858C>G
|
NP_004077.1:p.Gly286=
|
|
NR_038356.1:n.1347G>C
|
|
|
XM_011536539.1:c.858C>G
|
XP_011534841.1:p.Gly286=
|
|
NM_001347720.1:c.1053C>G
|
NP_001334649.1:p.Gly351=
|
|
XM_017021071.1:c.1053C>G
|
XP_016876560.1:p.Gly351=
|
|
XM_024449506.1:c.915C>G
|
XP_024305274.1:p.Gly305=
|
|
NM_004086.3:c.858C>G
MANE Select
|
NP_004077.1:p.Gly286=
|
|
NM_001135058.2:c.858C>G
|
NP_001128530.1:p.Gly286=
|
|
NM_001347720.2:c.1053C>G
|
NP_001334649.1:p.Gly351=
|
|