ENST00000532043.2:n.199G>T
|
|
|
ENST00000682266.1:c.1732G>T
|
ENSP00000507766.1:p.Gly578Cys
|
|
ENST00000682341.1:c.2140G>T
|
ENSP00000508251.1:p.Gly714Cys
|
|
ENST00000683197.1:c.2140G>T
|
ENSP00000507641.1:p.Gly714Cys
|
|
ENST00000683411.1:c.1732G>T
|
ENSP00000508397.1:p.Gly578Cys
|
|
ENST00000683437.1:c.1732G>T
|
ENSP00000508408.1:p.Gly578Cys
|
|
ENST00000683613.1:n.3176G>T
|
|
|
ENST00000684663.1:c.2137G>T
|
ENSP00000508009.1:p.Gly713Cys
|
|
ENST00000324559.9:c.2182G>T
MANE Select
|
ENSP00000315371.9:p.Gly728Cys
|
|
ENST00000648804.1:n.2517G>T
|
|
|
ENST00000324559.8:c.2182G>T
|
ENSP00000315371.8:p.Gly728Cys
|
|
ENST00000532043.1:n.199G>T
|
|
|
NM_001142649.1:c.2179G>T
|
NP_001136121.1:p.Gly727Cys
|
|
NM_213599.2:c.2182G>T , LRG_868t1:c.2182G>T
|
NP_998764.1:p.Gly728Cys
|
|
XM_005252820.2:c.2140G>T
|
XP_005252877.2:p.Gly714Cys
|
|
XM_005252821.2:c.2137G>T
|
XP_005252878.2:p.Gly713Cys
|
|
XM_005252822.3:c.2104G>T
|
XP_005252879.1:p.Gly702Cys
|
|
XM_005252823.3:c.2101G>T
|
XP_005252880.1:p.Gly701Cys
|
|
XM_011519949.1:c.2089G>T
|
XP_011518251.1:p.Gly697Cys
|
|
XM_005252820.3:c.2140G>T
|
XP_005252877.2:p.Gly714Cys
|
|
XM_005252821.3:c.2137G>T
|
XP_005252878.2:p.Gly713Cys
|
|
XM_005252822.4:c.2104G>T
|
XP_005252879.1:p.Gly702Cys
|
|
XM_011519949.2:c.2089G>T
|
XP_011518251.1:p.Gly697Cys
|
|
NM_001142649.2:c.2179G>T
|
NP_001136121.1:p.Gly727Cys
|
|
NM_213599.3:c.2182G>T
MANE Select
|
NP_998764.1:p.Gly728Cys
|
|