ENST00000299314.12:c.3561G>T
MANE Select
|
ENSP00000299314.7:p.Glu1187Asp
|
|
ENST00000299314.11:c.3561G>T
|
ENSP00000299314.7:p.Glu1187Asp
|
|
ENST00000549738.5:c.459G>T
|
ENSP00000450161.1:n.459G>T
|
|
NM_024312.4:c.3561G>T
|
NP_077288.2:p.Glu1187Asp
|
|
XM_011538731.1:c.3480G>T
|
XP_011537033.1:p.Glu1160Asp
|
|
XM_011538731.2:c.3480G>T
|
XP_011537033.1:p.Glu1160Asp
|
|
XM_017019961.1:c.3345G>T
|
XP_016875450.1:p.Glu1115Asp
|
|
XM_017019962.2:c.2334G>T
|
XP_016875451.1:p.Glu778Asp
|
|
NM_024312.5:c.3561G>T
MANE Select
|
NP_077288.2:p.Glu1187Asp
|
|