ENST00000465125.2:c.1462G>T
|
ENSP00000515651.1:p.Gly488Ter
|
|
ENST00000400908.7:c.3124G>T
MANE Select
|
ENSP00000383700.2:p.Gly1042Ter
|
|
ENST00000337907.7:c.3124G>T
|
ENSP00000338629.3:p.Gly1042Ter
|
|
ENST00000377464.5:c.2320G>T
|
ENSP00000366684.1:p.Gly774Ter
|
|
ENST00000400907.6:c.1540+4363G>T
|
ENSP00000383699.2:n.1540+4363G>T
|
|
ENST00000400908.6:c.3124G>T
|
ENSP00000383700.2:p.Gly1042Ter
|
|
ENST00000476556.5:c.1462G>T
|
ENSP00000422246.1:p.Gly488Ter
|
|
ENST00000505225.1:c.307+1077G>T
|
ENSP00000423451.1:n.307+1077G>T
|
|
NM_001042681.1:c.3124G>T
|
NP_001036146.1:p.Gly1042Ter
|
|
NM_001042682.1:c.1462G>T
|
NP_001036147.1:p.Gly488Ter
|
|
NM_012102.3:c.3124G>T
|
NP_036234.3:p.Gly1042Ter
|
|
XM_005263464.1:c.3124G>T
|
XP_005263521.1:p.Gly1042Ter
|
|
XM_005263466.1:c.2320G>T
|
XP_005263523.1:p.Gly774Ter
|
|
XM_006710653.1:c.3124G>T
|
XP_006710716.1:p.Gly1042Ter
|
|
XM_011541510.1:c.2998G>T
|
XP_011539812.1:p.Gly1000Ter
|
|
XM_011541511.1:c.3124G>T
|
XP_011539813.1:p.Gly1042Ter
|
|
XM_005263464.2:c.3124G>T
|
XP_005263521.1:p.Gly1042Ter
|
|
XM_011541510.2:c.2998G>T
|
XP_011539812.1:p.Gly1000Ter
|
|
XM_011541511.2:c.3124G>T
|
XP_011539813.1:p.Gly1042Ter
|
|
XM_017001358.1:c.3124G>T
|
XP_016856847.1:p.Gly1042Ter
|
|
XM_017001359.1:c.3124G>T
|
XP_016856848.1:p.Gly1042Ter
|
|
NM_001042681.2:c.3124G>T
MANE Select
|
NP_001036146.1:p.Gly1042Ter
|
|
NM_001042682.2:c.1462G>T
|
NP_001036147.1:p.Gly488Ter
|
|
NM_012102.4:c.3124G>T
|
NP_036234.3:p.Gly1042Ter
|
|