ENST00000346342.8:c.1297C>A
MANE Select
|
ENSP00000329546.4:p.Pro433Thr
|
|
ENST00000346342.7:c.1297C>A
|
ENSP00000329546.3:p.Pro433Thr
|
|
ENST00000375581.3:c.1363C>A
|
ENSP00000364731.3:p.Pro455Thr
|
|
ENST00000541084.5:c.1111C>A
|
ENSP00000442051.2:p.Pro371Thr
|
|
NM_000131.4:c.1363C>A , LRG_554t1:c.1363C>A
|
NP_000122.1:p.Pro455Thr
|
|
NM_001267554.1:c.1111C>A
|
NP_001254483.1:p.Pro371Thr
|
|
NM_019616.3:c.1297C>A , LRG_554t2:c.1297C>A
|
NP_062562.1:p.Pro433Thr
|
|
NR_051961.1:n.1384C>A
|
|
|
XM_006719963.2:c.1156C>A
|
XP_006720026.1:p.Pro386Thr
|
|
XM_011537474.1:c.1405C>A
|
XP_011535776.1:p.Pro469Thr
|
|
XM_011537475.1:c.1219C>A
|
XP_011535777.1:p.Pro407Thr
|
|
XM_011537476.1:c.1057C>A
|
XP_011535778.1:p.Pro353Thr
|
|
XM_011537477.1:c.1366C>A
|
XP_011535779.1:p.Pro456Thr
|
|
XM_006719963.3:c.1201C>A
|
XP_006720026.2:p.Pro401Thr
|
|
XM_011537474.2:c.1450C>A
|
XP_011535776.2:p.Pro484Thr
|
|
XM_011537475.2:c.1264C>A
|
XP_011535777.2:p.Pro422Thr
|
|
XM_011537476.2:c.1057C>A
|
XP_011535778.1:p.Pro353Thr
|
|
NM_019616.4:c.1297C>A
MANE Select
|
NP_062562.1:p.Pro433Thr
|
|
NR_051961.2:n.1381C>A
|
|
|
NM_001267554.2:c.1111C>A
|
NP_001254483.1:p.Pro371Thr
|
|