ENST00000346342.8:c.809G>C
MANE Select
|
ENSP00000329546.4:p.Ser270Thr
|
|
ENST00000346342.7:c.809G>C
|
ENSP00000329546.3:p.Ser270Thr
|
|
ENST00000375581.3:c.875G>C
|
ENSP00000364731.3:p.Ser292Thr
|
|
ENST00000541084.5:c.623G>C
|
ENSP00000442051.2:p.Ser208Thr
|
|
NM_000131.4:c.875G>C , LRG_554t1:c.875G>C
|
NP_000122.1:p.Ser292Thr
|
|
NM_001267554.1:c.623G>C
|
NP_001254483.1:p.Ser208Thr
|
|
NM_019616.3:c.809G>C , LRG_554t2:c.809G>C
|
NP_062562.1:p.Ser270Thr
|
|
NR_051961.1:n.896G>C
|
|
|
XM_006719963.2:c.668G>C
|
XP_006720026.1:p.Ser223Thr
|
|
XM_011537474.1:c.917G>C
|
XP_011535776.1:p.Ser306Thr
|
|
XM_011537475.1:c.731G>C
|
XP_011535777.1:p.Ser244Thr
|
|
XM_011537476.1:c.569G>C
|
XP_011535778.1:p.Ser190Thr
|
|
XM_011537477.1:c.878G>C
|
XP_011535779.1:p.Ser293Thr
|
|
XM_006719963.3:c.713G>C
|
XP_006720026.2:p.Ser238Thr
|
|
XM_011537474.2:c.962G>C
|
XP_011535776.2:p.Ser321Thr
|
|
XM_011537475.2:c.776G>C
|
XP_011535777.2:p.Ser259Thr
|
|
XM_011537476.2:c.569G>C
|
XP_011535778.1:p.Ser190Thr
|
|
NM_019616.4:c.809G>C
MANE Select
|
NP_062562.1:p.Ser270Thr
|
|
NR_051961.2:n.893G>C
|
|
|
NM_001267554.2:c.623G>C
|
NP_001254483.1:p.Ser208Thr
|
|