ENST00000264595.7:c.551C>G
MANE Select
|
ENSP00000264595.2:p.Pro184Arg
|
|
ENST00000264595.6:c.551C>G
|
ENSP00000264595.2:p.Pro184Arg
|
|
ENST00000502310.5:c.206C>G
|
ENSP00000423798.1:p.Pro69Arg
|
|
ENST00000506853.5:n.585C>G
|
|
|
ENST00000510635.1:c.247C>G
|
|
|
ENST00000510955.5:n.472C>G
|
|
|
NM_000027.3:c.551C>G
|
NP_000018.2:p.Pro184Arg
|
|
NM_001171988.1:c.551C>G
|
NP_001165459.1:p.Pro184Arg
|
|
NR_033655.1:n.679C>G
|
|
|
XM_006714123.2:c.551C>G
|
XP_006714186.1:p.Pro184Arg
|
|
XR_001741155.2:n.645C>G
|
|
|
NM_000027.4:c.551C>G
MANE Select
|
NP_000018.2:p.Pro184Arg
|
|
NM_001171988.2:c.551C>G
|
NP_001165459.1:p.Pro184Arg
|
|
NR_033655.2:n.613C>G
|
|
|