ENST00000673739.2:c.*2805T>G
|
ENSP00000501110.2:n.*2805T>G
|
|
ENST00000673882.2:c.*2594T>G
|
ENSP00000501253.2:n.*2594T>G
|
|
ENST00000673739.1:c.3213T>G
|
ENSP00000501110.1:n.3213T>G
|
|
ENST00000673882.1:c.3002T>G
|
ENSP00000501253.1:n.3002T>G
|
|
ENST00000233242.5:c.3499T>G
MANE Select
|
ENSP00000233242.1:p.Trp1167Gly
|
|
ENST00000616098.4:c.3499T>G
|
ENSP00000477990.1:p.Trp1167Gly
|
|
NM_000384.2:c.3499T>G
|
NP_000375.2:p.Trp1167Gly
|
|
XM_011532809.1:c.3499T>G
|
XP_011531111.1:p.Trp1167Gly
|
|
NM_000384.3:c.3499T>G
MANE Select
|
NP_000375.3:p.Trp1167Gly
|
|