ENST00000371269.9:c.1412A>C
MANE Select
|
ENSP00000360316.3:p.Tyr471Ser
|
|
ENST00000436604.2:c.1412A>C
|
ENSP00000416585.2:p.Tyr471Ser
|
|
ENST00000535035.6:c.1448A>C
|
ENSP00000440191.3:p.Tyr483Ser
|
|
ENST00000647585.1:n.1216A>C
|
|
|
ENST00000647912.1:c.*1047A>C
|
ENSP00000497559.1:n.*1047A>C
|
|
ENST00000648712.1:n.1530A>C
|
|
|
ENST00000648728.1:c.*1067A>C
|
ENSP00000497084.1:n.*1067A>C
|
|
ENST00000649769.1:c.*2114A>C
|
ENSP00000498012.1:n.*2114A>C
|
|
ENST00000371269.7:c.1412A>C
|
ENSP00000360316.3:p.Tyr471Ser
|
|
ENST00000436604.1:c.324A>C
|
|
|
ENST00000535035.5:c.1145A>C
|
ENSP00000440191.2:p.Tyr382Ser
|
|
NM_014762.3:c.1412A>C
|
NP_055577.1:p.Tyr471Ser
|
|
NM_014762.4:c.1412A>C
MANE Select
|
NP_055577.1:p.Tyr471Ser
|
|