ENST00000281182.9:c.1147G>T
MANE Select
|
ENSP00000281182.5:p.Ala383Ser
|
|
ENST00000281182.8:c.1147G>T
|
ENSP00000281182.4:p.Ala383Ser
|
|
ENST00000374752.6:c.766G>T
|
ENSP00000363884.4:p.Ala256Ser
|
|
ENST00000524426.5:c.*877G>T
|
ENSP00000431310.1:n.*877G>T
|
|
ENST00000524502.2:n.147G>T
|
|
|
ENST00000526026.5:c.*836G>T
|
ENSP00000431532.1:n.*836G>T
|
|
ENST00000531338.5:n.1391G>T
|
|
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ENST00000533387.5:n.2206G>T
|
|
|
NM_014384.2:c.1147G>T , LRG_448t1:c.1147G>T
|
NP_055199.1:p.Ala383Ser
|
|
XM_005271501.2:c.1147G>T
|
XP_005271558.1:p.Ala383Ser
|
|
XM_011542750.1:c.1147G>T
|
XP_011541052.1:p.Ala383Ser
|
|
XR_947819.1:n.1211G>T
|
|
|
XR_947820.1:n.1599G>T
|
|
|
XR_947821.1:n.1356G>T
|
|
|
XR_947822.1:n.1041G>T
|
|
|
XR_947823.1:n.1197G>T
|
|
|
XM_005271505.4:c.*1412G>T
|
XP_005271562.1:n.*1412G>T
|
|
XM_011542750.3:c.1147G>T
|
XP_011541052.1:p.Ala383Ser
|
|
XM_017017542.2:c.1147G>T
|
XP_016873031.1:p.Ala383Ser
|
|
XM_017017543.2:c.1147G>T
|
XP_016873032.1:p.Ala383Ser
|
|
XM_017017544.2:c.*116G>T
|
XP_016873033.1:n.*116G>T
|
|
XM_017017545.2:c.*359G>T
|
XP_016873034.1:n.*359G>T
|
|
XM_017017546.2:c.853G>T
|
XP_016873035.1:p.Ala285Ser
|
|
XM_017017547.2:c.853G>T
|
XP_016873036.1:p.Ala285Ser
|
|
XM_017017548.2:c.*1783G>T
|
XP_016873037.1:n.*1783G>T
|
|
XM_017017549.2:c.*1557G>T
|
XP_016873038.1:n.*1557G>T
|
|
XM_024448437.1:c.*294G>T
|
XP_024304205.1:n.*294G>T
|
|
XM_024448438.1:c.766G>T
|
XP_024304206.1:p.Ala256Ser
|
|
NM_014384.3:c.1147G>T
MANE Select
|
NP_055199.1:p.Ala383Ser
|
|