ENST00000346342.8:c.1290C>T
MANE Select
|
ENSP00000329546.4:p.Arg430=
|
|
ENST00000346342.7:c.1290C>T
|
ENSP00000329546.3:p.Arg430=
|
|
ENST00000375581.3:c.1356C>T
|
ENSP00000364731.3:p.Arg452=
|
|
ENST00000541084.5:c.1104C>T
|
ENSP00000442051.2:p.Arg368=
|
|
NM_000131.4:c.1356C>T , LRG_554t1:c.1356C>T
|
NP_000122.1:p.Arg452=
|
|
NM_001267554.1:c.1104C>T
|
NP_001254483.1:p.Arg368=
|
|
NM_019616.3:c.1290C>T , LRG_554t2:c.1290C>T
|
NP_062562.1:p.Arg430=
|
|
NR_051961.1:n.1377C>T
|
|
|
XM_006719963.2:c.1149C>T
|
XP_006720026.1:p.Arg383=
|
|
XM_011537474.1:c.1398C>T
|
XP_011535776.1:p.Arg466=
|
|
XM_011537475.1:c.1212C>T
|
XP_011535777.1:p.Arg404=
|
|
XM_011537476.1:c.1050C>T
|
XP_011535778.1:p.Arg350=
|
|
XM_011537477.1:c.1359C>T
|
XP_011535779.1:p.Arg453=
|
|
XM_006719963.3:c.1194C>T
|
XP_006720026.2:p.Arg398=
|
|
XM_011537474.2:c.1443C>T
|
XP_011535776.2:p.Arg481=
|
|
XM_011537475.2:c.1257C>T
|
XP_011535777.2:p.Arg419=
|
|
XM_011537476.2:c.1050C>T
|
XP_011535778.1:p.Arg350=
|
|
NM_019616.4:c.1290C>T
MANE Select
|
NP_062562.1:p.Arg430=
|
|
NR_051961.2:n.1374C>T
|
|
|
NM_001267554.2:c.1104C>T
|
NP_001254483.1:p.Arg368=
|
|