ENST00000243964.7:c.3078T>C
MANE Select
|
ENSP00000243964.4:p.Ser1026=
|
|
ENST00000243964.6:c.3078T>C
|
ENSP00000243964.3:p.Ser1026=
|
|
ENST00000454036.6:c.3147T>C
|
ENSP00000387694.1:p.Ser1049=
|
|
ENST00000616201.4:c.1298-2124T>C
|
ENSP00000484585.1:n.1298-2124T>C
|
|
ENST00000616202.4:c.613-1949T>C
|
ENSP00000478369.1:n.613-1949T>C
|
|
ENST00000616933.4:c.*2396T>C
|
ENSP00000477569.1:n.*2396T>C
|
|
ENST00000626937.2:c.510-3067T>C
|
ENSP00000485953.1:n.510-3067T>C
|
|
NM_001134771.1:c.3147T>C
|
NP_001128243.1:p.Ser1049=
|
|
NM_020708.4:c.3078T>C
|
NP_065759.1:p.Ser1026=
|
|
XM_017027981.1:c.3147T>C
|
XP_016883470.1:p.Ser1049=
|
|
NM_001134771.2:c.3147T>C
|
NP_001128243.1:p.Ser1049=
|
|
NM_020708.5:c.3078T>C
MANE Select
|
NP_065759.1:p.Ser1026=
|
|