ENST00000368373.8:c.570G>T
MANE Select
|
ENSP00000357357.3:p.Glu190Asp
|
|
ENST00000327247.9:c.570G>T
|
ENSP00000314508.5:p.Glu190Asp
|
|
ENST00000368373.7:c.570G>T
|
ENSP00000357357.3:p.Glu190Asp
|
|
ENST00000427500.7:c.423G>T
|
ENSP00000402577.2:p.Glu141Asp
|
|
ENST00000428024.3:c.309G>T
|
ENSP00000397986.2:p.Glu103Asp
|
|
ENST00000460156.1:n.357G>T
|
|
|
ENST00000484489.5:n.339+1438G>T
|
|
|
ENST00000491081.5:n.175G>T
|
|
|
ENST00000493842.5:n.908G>T
|
|
|
ENST00000497670.5:n.193G>T
|
|
|
NM_000157.3:c.570G>T
|
NP_000148.2:p.Glu190Asp
|
|
NM_001005741.2:c.570G>T
|
NP_001005741.1:p.Glu190Asp
|
|
NM_001005742.2:c.570G>T
|
NP_001005742.1:p.Glu190Asp
|
|
NM_001171811.1:c.309G>T
|
NP_001165282.1:p.Glu103Asp
|
|
NM_001171812.1:c.423G>T
|
NP_001165283.1:p.Glu141Asp
|
|
XM_006711270.1:c.570G>T
|
XP_006711333.1:p.Glu190Asp
|
|
XM_011509407.1:c.570G>T
|
XP_011507709.1:p.Glu190Asp
|
|
NM_000157.4:c.570G>T
MANE Select
|
NP_000148.2:p.Glu190Asp
|
|
NM_001005741.3:c.570G>T
|
NP_001005741.1:p.Glu190Asp
|
|
NM_001005742.3:c.570G>T
|
NP_001005742.1:p.Glu190Asp
|
|
NM_001171811.2:c.309G>T
|
NP_001165282.1:p.Glu103Asp
|
|
NM_001171812.2:c.423G>T
|
NP_001165283.1:p.Glu141Asp
|
|