ENST00000346342.8:c.806C>A
MANE Select
|
ENSP00000329546.4:p.Pro269His
|
|
ENST00000346342.7:c.806C>A
|
ENSP00000329546.3:p.Pro269His
|
|
ENST00000375581.3:c.872C>A
|
ENSP00000364731.3:p.Pro291His
|
|
ENST00000541084.5:c.620C>A
|
ENSP00000442051.2:p.Pro207His
|
|
NM_000131.4:c.872C>A , LRG_554t1:c.872C>A
|
NP_000122.1:p.Pro291His
|
|
NM_001267554.1:c.620C>A
|
NP_001254483.1:p.Pro207His
|
|
NM_019616.3:c.806C>A , LRG_554t2:c.806C>A
|
NP_062562.1:p.Pro269His
|
|
NR_051961.1:n.893C>A
|
|
|
XM_006719963.2:c.665C>A
|
XP_006720026.1:p.Pro222His
|
|
XM_011537474.1:c.914C>A
|
XP_011535776.1:p.Pro305His
|
|
XM_011537475.1:c.728C>A
|
XP_011535777.1:p.Pro243His
|
|
XM_011537476.1:c.566C>A
|
XP_011535778.1:p.Pro189His
|
|
XM_011537477.1:c.875C>A
|
XP_011535779.1:p.Pro292His
|
|
XM_006719963.3:c.710C>A
|
XP_006720026.2:p.Pro237His
|
|
XM_011537474.2:c.959C>A
|
XP_011535776.2:p.Pro320His
|
|
XM_011537475.2:c.773C>A
|
XP_011535777.2:p.Pro258His
|
|
XM_011537476.2:c.566C>A
|
XP_011535778.1:p.Pro189His
|
|
NM_019616.4:c.806C>A
MANE Select
|
NP_062562.1:p.Pro269His
|
|
NR_051961.2:n.890C>A
|
|
|
NM_001267554.2:c.620C>A
|
NP_001254483.1:p.Pro207His
|
|