ENST00000368373.8:c.566C>A
MANE Select
|
ENSP00000357357.3:p.Pro189Gln
|
|
ENST00000327247.9:c.566C>A
|
ENSP00000314508.5:p.Pro189Gln
|
|
ENST00000368373.7:c.566C>A
|
ENSP00000357357.3:p.Pro189Gln
|
|
ENST00000427500.7:c.419C>A
|
ENSP00000402577.2:p.Pro140Gln
|
|
ENST00000428024.3:c.305C>A
|
ENSP00000397986.2:p.Pro102Gln
|
|
ENST00000460156.1:n.353C>A
|
|
|
ENST00000484489.5:n.339+1434C>A
|
|
|
ENST00000491081.5:n.171C>A
|
|
|
ENST00000493842.5:n.904C>A
|
|
|
ENST00000497670.5:n.189C>A
|
|
|
NM_000157.3:c.566C>A
|
NP_000148.2:p.Pro189Gln
|
|
NM_001005741.2:c.566C>A
|
NP_001005741.1:p.Pro189Gln
|
|
NM_001005742.2:c.566C>A
|
NP_001005742.1:p.Pro189Gln
|
|
NM_001171811.1:c.305C>A
|
NP_001165282.1:p.Pro102Gln
|
|
NM_001171812.1:c.419C>A
|
NP_001165283.1:p.Pro140Gln
|
|
XM_006711270.1:c.566C>A
|
XP_006711333.1:p.Pro189Gln
|
|
XM_011509407.1:c.566C>A
|
XP_011507709.1:p.Pro189Gln
|
|
NM_000157.4:c.566C>A
MANE Select
|
NP_000148.2:p.Pro189Gln
|
|
NM_001005741.3:c.566C>A
|
NP_001005741.1:p.Pro189Gln
|
|
NM_001005742.3:c.566C>A
|
NP_001005742.1:p.Pro189Gln
|
|
NM_001171811.2:c.305C>A
|
NP_001165282.1:p.Pro102Gln
|
|
NM_001171812.2:c.419C>A
|
NP_001165283.1:p.Pro140Gln
|
|