ENST00000346342.8:c.1323C>G
MANE Select
|
ENSP00000329546.4:p.Ala441=
|
|
ENST00000346342.7:c.1323C>G
|
ENSP00000329546.3:p.Ala441=
|
|
ENST00000375581.3:c.1389C>G
|
ENSP00000364731.3:p.Ala463=
|
|
ENST00000541084.5:c.1137C>G
|
ENSP00000442051.2:p.Ala379=
|
|
NM_000131.4:c.1389C>G , LRG_554t1:c.1389C>G
|
NP_000122.1:p.Ala463=
|
|
NM_001267554.1:c.1137C>G
|
NP_001254483.1:p.Ala379=
|
|
NM_019616.3:c.1323C>G , LRG_554t2:c.1323C>G
|
NP_062562.1:p.Ala441=
|
|
NR_051961.1:n.1410C>G
|
|
|
XM_006719963.2:c.1182C>G
|
XP_006720026.1:p.Ala394=
|
|
XM_011537474.1:c.1431C>G
|
XP_011535776.1:p.Ala477=
|
|
XM_011537475.1:c.1245C>G
|
XP_011535777.1:p.Ala415=
|
|
XM_011537476.1:c.1083C>G
|
XP_011535778.1:p.Ala361=
|
|
XM_011537477.1:c.1392C>G
|
XP_011535779.1:p.Ala464=
|
|
XM_006719963.3:c.1227C>G
|
XP_006720026.2:p.Ala409=
|
|
XM_011537474.2:c.1476C>G
|
XP_011535776.2:p.Ala492=
|
|
XM_011537475.2:c.1290C>G
|
XP_011535777.2:p.Ala430=
|
|
XM_011537476.2:c.1083C>G
|
XP_011535778.1:p.Ala361=
|
|
NM_019616.4:c.1323C>G
MANE Select
|
NP_062562.1:p.Ala441=
|
|
NR_051961.2:n.1407C>G
|
|
|
NM_001267554.2:c.1137C>G
|
NP_001254483.1:p.Ala379=
|
|