ENST00000346342.8:c.1134C>T
MANE Select
|
ENSP00000329546.4:p.Cys378=
|
|
ENST00000346342.7:c.1134C>T
|
ENSP00000329546.3:p.Cys378=
|
|
ENST00000375581.3:c.1200C>T
|
ENSP00000364731.3:p.Cys400=
|
|
ENST00000541084.5:c.948C>T
|
ENSP00000442051.2:p.Cys316=
|
|
NM_000131.4:c.1200C>T , LRG_554t1:c.1200C>T
|
NP_000122.1:p.Cys400=
|
|
NM_001267554.1:c.948C>T
|
NP_001254483.1:p.Cys316=
|
|
NM_019616.3:c.1134C>T , LRG_554t2:c.1134C>T
|
NP_062562.1:p.Cys378=
|
|
NR_051961.1:n.1221C>T
|
|
|
XM_006719963.2:c.993C>T
|
XP_006720026.1:p.Cys331=
|
|
XM_011537474.1:c.1242C>T
|
XP_011535776.1:p.Cys414=
|
|
XM_011537475.1:c.1056C>T
|
XP_011535777.1:p.Cys352=
|
|
XM_011537476.1:c.894C>T
|
XP_011535778.1:p.Cys298=
|
|
XM_011537477.1:c.1203C>T
|
XP_011535779.1:p.Cys401=
|
|
XM_006719963.3:c.1038C>T
|
XP_006720026.2:p.Cys346=
|
|
XM_011537474.2:c.1287C>T
|
XP_011535776.2:p.Cys429=
|
|
XM_011537475.2:c.1101C>T
|
XP_011535777.2:p.Cys367=
|
|
XM_011537476.2:c.894C>T
|
XP_011535778.1:p.Cys298=
|
|
NM_019616.4:c.1134C>T
MANE Select
|
NP_062562.1:p.Cys378=
|
|
NR_051961.2:n.1218C>T
|
|
|
NM_001267554.2:c.948C>T
|
NP_001254483.1:p.Cys316=
|
|