|
ENST00000326735.13:c.1217G>T
MANE Select
|
ENSP00000327214.8:p.Gly406Val
|
|
|
ENST00000326735.12:c.1217G>T
|
ENSP00000327214.8:p.Gly406Val
|
|
|
ENST00000341676.9:c.1202G>T
|
ENSP00000341115.5:p.Gly401Val
|
|
|
ENST00000452699.5:c.1202G>T
|
ENSP00000413307.1:p.Gly401Val
|
|
|
ENST00000463860.5:n.825G>T
|
|
|
|
ENST00000502860.1:n.335-175G>T
|
|
|
|
ENST00000506174.5:c.359G>T
|
ENSP00000424393.1:p.Gly120Val
|
|
|
ENST00000509392.1:n.220G>T
|
|
|
|
ENST00000617114.4:c.335-175G>T
|
ENSP00000478781.1:n.335-175G>T
|
|
|
NM_001141973.2:c.1202G>T
|
NP_001135445.1:p.Gly401Val
|
|
|
NM_001141974.2:c.1202G>T
|
NP_001135446.1:p.Gly401Val
|
|
|
NM_022089.3:c.1217G>T
|
NP_071372.1:p.Gly406Val
|
|
|
XM_005245809.1:c.1217G>T
|
XP_005245866.1:p.Gly406Val
|
|
|
XM_005245810.1:c.1214G>T
|
XP_005245867.1:p.Gly405Val
|
|
|
XM_005245811.1:c.1202G>T
|
XP_005245868.1:p.Gly401Val
|
|
|
XM_005245812.1:c.1190G>T
|
XP_005245869.1:p.Gly397Val
|
|
|
XM_005245813.1:c.1217G>T
|
XP_005245870.1:p.Gly406Val
|
|
|
XM_005245815.1:c.1217G>T
|
XP_005245872.1:p.Gly406Val
|
|
|
XM_006710512.1:c.1199G>T
|
XP_006710575.1:p.Gly400Val
|
|
|
XM_006710513.1:c.1175G>T
|
XP_006710576.1:p.Gly392Val
|
|
|
XM_011541128.1:c.1217G>T
|
XP_011539430.1:p.Gly406Val
|
|
|
XM_011541129.1:c.1217G>T
|
XP_011539431.1:p.Gly406Val
|
|
|
XM_017000844.1:c.1217G>T
|
XP_016856333.1:p.Gly406Val
|
|
|
XM_017000845.1:c.1199G>T
|
XP_016856334.1:p.Gly400Val
|
|
|
XM_017000846.1:c.1175G>T
|
XP_016856335.1:p.Gly392Val
|
|
|
XM_017000847.1:c.1187G>T
|
XP_016856336.1:p.Gly396Val
|
|
|
XM_017000848.1:c.1217G>T
|
XP_016856337.1:p.Gly406Val
|
|
|
XM_017000849.1:c.1202G>T
|
XP_016856338.1:p.Gly401Val
|
|
|
XM_017000850.1:c.1217G>T
|
XP_016856339.1:p.Gly406Val
|
|
|
NM_022089.4:c.1217G>T
MANE Select
|
NP_071372.1:p.Gly406Val
|
|
|
NM_001141973.3:c.1202G>T
|
NP_001135445.1:p.Gly401Val
|
|
|
NM_001141974.3:c.1202G>T
|
NP_001135446.1:p.Gly401Val
|
|
