ENST00000346342.8:c.1047G=
MANE Select
|
ENSP00000329546.4:p.Leu349=
|
|
ENST00000346342.7:c.1047G=
|
ENSP00000329546.3:p.Leu349=
|
|
ENST00000375581.3:c.1113G=
|
ENSP00000364731.3:p.Leu371=
|
|
ENST00000541084.5:c.861G=
|
ENSP00000442051.2:p.Leu287=
|
|
NM_000131.4:c.1113G= , LRG_554t1:c.1113G=
|
NP_000122.1:p.Leu371=
|
|
NM_001267554.1:c.861G=
|
NP_001254483.1:p.Leu287=
|
|
NM_019616.3:c.1047G= , LRG_554t2:c.1047G=
|
NP_062562.1:p.Leu349=
|
|
NR_051961.1:n.1134G=
|
|
|
XM_006719963.2:c.906G=
|
XP_006720026.1:p.Leu302=
|
|
XM_011537474.1:c.1155G=
|
XP_011535776.1:p.Leu385=
|
|
XM_011537475.1:c.969G=
|
XP_011535777.1:p.Leu323=
|
|
XM_011537476.1:c.807G=
|
XP_011535778.1:p.Leu269=
|
|
XM_011537477.1:c.1116G=
|
XP_011535779.1:p.Leu372=
|
|
XM_006719963.3:c.951G=
|
XP_006720026.2:p.Leu317=
|
|
XM_011537474.2:c.1200G=
|
XP_011535776.2:p.Leu400=
|
|
XM_011537475.2:c.1014G=
|
XP_011535777.2:p.Leu338=
|
|
XM_011537476.2:c.807G=
|
XP_011535778.1:p.Leu269=
|
|
NM_019616.4:c.1047G=
MANE Select
|
NP_062562.1:p.Leu349=
|
|
NR_051961.2:n.1131G=
|
|
|
NM_001267554.2:c.861G=
|
NP_001254483.1:p.Leu287=
|
|