ENST00000361915.8:c.3770G>A
MANE Select
|
ENSP00000355106.3:p.Gly1257Asp
|
|
ENST00000637337.1:n.3981G>A
|
|
|
ENST00000294724.8:c.3770G>A
|
ENSP00000294724.4:p.Gly1257Asp
|
|
ENST00000361302.7:c.3722G>A
|
ENSP00000354971.3:p.Gly1241Asp
|
|
ENST00000361522.4:c.3719G>A
|
ENSP00000354635.4:p.Gly1240Asp
|
|
ENST00000361915.7:c.3770G>A
|
ENSP00000355106.3:p.Gly1257Asp
|
|
ENST00000370161.6:c.3722G>A
|
ENSP00000359180.2:p.Gly1241Asp
|
|
ENST00000370163.7:c.3770G>A
|
ENSP00000359182.3:p.Gly1257Asp
|
|
ENST00000370165.7:c.3770G>A
|
ENSP00000359184.3:p.Gly1257Asp
|
|
NM_000028.2:c.3770G>A
|
NP_000019.2:p.Gly1257Asp
|
|
NM_000642.2:c.3770G>A
|
NP_000633.2:p.Gly1257Asp
|
|
NM_000643.2:c.3770G>A
|
NP_000634.2:p.Gly1257Asp
|
|
NM_000644.2:c.3770G>A
|
NP_000635.2:p.Gly1257Asp
|
|
NM_000645.2:c.3719G>A
|
NP_000636.2:p.Gly1240Asp
|
|
NM_000646.2:c.3722G>A
|
NP_000637.2:p.Gly1241Asp
|
|
XM_005270557.1:c.3770G>A
|
XP_005270614.1:p.Gly1257Asp
|
|
XM_005270557.2:c.3770G>A
|
XP_005270614.1:p.Gly1257Asp
|
|
XM_017000501.2:c.2030G>A
|
XP_016855990.1:p.Gly677Asp
|
|
NM_000642.3:c.3770G>A
MANE Select
|
NP_000633.2:p.Gly1257Asp
|
|