ENST00000243964.7:c.2803G>T
MANE Select
|
ENSP00000243964.4:p.Asp935Tyr
|
|
ENST00000243964.6:c.2803G>T
|
ENSP00000243964.3:p.Asp935Tyr
|
|
ENST00000454036.6:c.2872G>T
|
ENSP00000387694.1:p.Asp958Tyr
|
|
ENST00000616201.4:c.1298-2491G>T
|
ENSP00000484585.1:n.1298-2491G>T
|
|
ENST00000616202.4:c.613-2316G>T
|
ENSP00000478369.1:n.613-2316G>T
|
|
ENST00000616933.4:c.*2121G>T
|
ENSP00000477569.1:n.*2121G>T
|
|
ENST00000626937.2:c.510-3434G>T
|
ENSP00000485953.1:n.510-3434G>T
|
|
ENST00000628413.1:n.319G>T
|
|
|
NM_001134771.1:c.2872G>T
|
NP_001128243.1:p.Asp958Tyr
|
|
NM_020708.4:c.2803G>T
|
NP_065759.1:p.Asp935Tyr
|
|
XM_017027981.1:c.2872G>T
|
XP_016883470.1:p.Asp958Tyr
|
|
NM_001134771.2:c.2872G>T
|
NP_001128243.1:p.Asp958Tyr
|
|
NM_020708.5:c.2803G>T
MANE Select
|
NP_065759.1:p.Asp935Tyr
|
|