ENST00000299314.12:c.1317C>A
MANE Select
|
ENSP00000299314.7:p.Ala439=
|
|
ENST00000299314.11:c.1317C>A
|
ENSP00000299314.7:p.Ala439=
|
|
ENST00000549940.5:c.1317C>A
|
ENSP00000449150.1:p.Ala439=
|
|
NM_024312.4:c.1317C>A
|
NP_077288.2:p.Ala439=
|
|
XM_006719593.2:c.1317C>A
|
XP_006719656.1:p.Ala439=
|
|
XM_011538731.1:c.1236C>A
|
XP_011537033.1:p.Ala412=
|
|
XM_006719593.3:c.1317C>A
|
XP_006719656.1:p.Ala439=
|
|
XM_011538731.2:c.1236C>A
|
XP_011537033.1:p.Ala412=
|
|
XM_017019961.1:c.1101C>A
|
XP_016875450.1:p.Ala367=
|
|
XM_017019962.2:c.90C>A
|
XP_016875451.1:p.Ala30=
|
|
NM_024312.5:c.1317C>A
MANE Select
|
NP_077288.2:p.Ala439=
|
|