|
NM_001080.3:c.851G>A
MANE Select
|
NP_001071.1:p.Gly284Asp
|
|
ENST00000357578.8:c.851G>A
MANE Select
|
ENSP00000350191.3:p.Gly284Asp
|
|
NM_001368954.1:c.727-5110G>A
|
NP_001355883.1:n.727-5110G>A
|
|
NM_170740.1:c.890G>A
|
NP_733936.1:p.Gly297Asp
|
|
ENST00000348925.2:c.890G>A
|
ENSP00000314649.3:p.Gly297Asp
|
|
ENST00000357578.7:c.851G>A
|
ENSP00000350191.3:p.Gly284Asp
|
|
ENST00000491546.5:c.767G>A
|
ENSP00000417687.1:p.Gly256Asp
|
|
ENST00000672352.1:c.490-5110G>A
|
ENSP00000500876.1:n.490-5110G>A
|
|
ENST00000672557.1:c.769G>A
|
|
|
ENST00000672619.1:n.211G>A
|
|
|
ENST00000672652.1:c.814G>A
|
|
|
ENST00000675422.1:n.1611G>A
|
|