ENST00000346342.8:c.767G>C
MANE Select
|
ENSP00000329546.4:p.Gly256Ala
|
|
ENST00000346342.7:c.767G>C
|
ENSP00000329546.3:p.Gly256Ala
|
|
ENST00000375581.3:c.833G>C
|
ENSP00000364731.3:p.Gly278Ala
|
|
ENST00000541084.5:c.581G>C
|
ENSP00000442051.2:p.Gly194Ala
|
|
NM_000131.4:c.833G>C , LRG_554t1:c.833G>C
|
NP_000122.1:p.Gly278Ala
|
|
NM_001267554.1:c.581G>C
|
NP_001254483.1:p.Gly194Ala
|
|
NM_019616.3:c.767G>C , LRG_554t2:c.767G>C
|
NP_062562.1:p.Gly256Ala
|
|
NR_051961.1:n.854G>C
|
|
|
XM_006719963.2:c.626G>C
|
XP_006720026.1:p.Gly209Ala
|
|
XM_011537474.1:c.875G>C
|
XP_011535776.1:p.Gly292Ala
|
|
XM_011537475.1:c.689G>C
|
XP_011535777.1:p.Gly230Ala
|
|
XM_011537476.1:c.527G>C
|
XP_011535778.1:p.Gly176Ala
|
|
XM_011537477.1:c.836G>C
|
XP_011535779.1:p.Gly279Ala
|
|
XM_006719963.3:c.671G>C
|
XP_006720026.2:p.Gly224Ala
|
|
XM_011537474.2:c.920G>C
|
XP_011535776.2:p.Gly307Ala
|
|
XM_011537475.2:c.734G>C
|
XP_011535777.2:p.Gly245Ala
|
|
XM_011537476.2:c.527G>C
|
XP_011535778.1:p.Gly176Ala
|
|
NM_019616.4:c.767G>C
MANE Select
|
NP_062562.1:p.Gly256Ala
|
|
NR_051961.2:n.851G>C
|
|
|
NM_001267554.2:c.581G>C
|
NP_001254483.1:p.Gly194Ala
|
|