ENST00000346342.8:c.318T=
MANE Select
|
ENSP00000329546.4:p.Tyr106=
|
|
ENST00000346342.7:c.318T=
|
ENSP00000329546.3:p.Tyr106=
|
|
ENST00000375581.3:c.384T=
|
ENSP00000364731.3:p.Tyr128=
|
|
ENST00000444337.1:c.*126T=
|
ENSP00000387669.1:n.*126T=
|
|
ENST00000473085.1:n.265T=
|
|
|
ENST00000479674.1:n.651T=
|
|
|
ENST00000541084.5:c.132T=
|
ENSP00000442051.2:p.Tyr44=
|
|
NM_000131.4:c.384T= , LRG_554t1:c.384T=
|
NP_000122.1:p.Tyr128=
|
|
NM_001267554.1:c.132T=
|
NP_001254483.1:p.Tyr44=
|
|
NM_019616.3:c.318T= , LRG_554t2:c.318T=
|
NP_062562.1:p.Tyr106=
|
|
NR_051961.1:n.405T=
|
|
|
XM_006719963.2:c.318T=
|
XP_006720026.1:p.Tyr106=
|
|
XM_011537474.1:c.318T=
|
XP_011535776.1:p.Tyr106=
|
|
XM_011537475.1:c.132T=
|
XP_011535777.1:p.Tyr44=
|
|
XM_011537477.1:c.279T=
|
XP_011535779.1:p.Tyr93=
|
|
XM_006719963.3:c.363T=
|
XP_006720026.2:p.Tyr121=
|
|
XM_011537474.2:c.363T=
|
XP_011535776.2:p.Tyr121=
|
|
XM_011537475.2:c.177T=
|
XP_011535777.2:p.Tyr59=
|
|
NM_019616.4:c.318T=
MANE Select
|
NP_062562.1:p.Tyr106=
|
|
NR_051961.2:n.402T=
|
|
|
NM_001267554.2:c.132T=
|
NP_001254483.1:p.Tyr44=
|
|