ENST00000346342.8:c.647G>C
MANE Select
|
ENSP00000329546.4:p.Cys216Ser
|
|
ENST00000346342.7:c.647G>C
|
ENSP00000329546.3:p.Cys216Ser
|
|
ENST00000375581.3:c.713G>C
|
ENSP00000364731.3:p.Cys238Ser
|
|
ENST00000541084.5:c.461G>C
|
ENSP00000442051.2:p.Cys154Ser
|
|
NM_000131.4:c.713G>C , LRG_554t1:c.713G>C
|
NP_000122.1:p.Cys238Ser
|
|
NM_001267554.1:c.461G>C
|
NP_001254483.1:p.Cys154Ser
|
|
NM_019616.3:c.647G>C , LRG_554t2:c.647G>C
|
NP_062562.1:p.Cys216Ser
|
|
NR_051961.1:n.734G>C
|
|
|
XM_006719963.2:c.506G>C
|
XP_006720026.1:p.Cys169Ser
|
|
XM_011537474.1:c.755G>C
|
XP_011535776.1:p.Cys252Ser
|
|
XM_011537475.1:c.569G>C
|
XP_011535777.1:p.Cys190Ser
|
|
XM_011537476.1:c.407G>C
|
XP_011535778.1:p.Cys136Ser
|
|
XM_011537477.1:c.716G>C
|
XP_011535779.1:p.Cys239Ser
|
|
XM_006719963.3:c.551G>C
|
XP_006720026.2:p.Cys184Ser
|
|
XM_011537474.2:c.800G>C
|
XP_011535776.2:p.Cys267Ser
|
|
XM_011537475.2:c.614G>C
|
XP_011535777.2:p.Cys205Ser
|
|
XM_011537476.2:c.407G>C
|
XP_011535778.1:p.Cys136Ser
|
|
NM_019616.4:c.647G>C
MANE Select
|
NP_062562.1:p.Cys216Ser
|
|
NR_051961.2:n.731G>C
|
|
|
NM_001267554.2:c.461G>C
|
NP_001254483.1:p.Cys154Ser
|
|