ENST00000313468.10:c.455A>G
MANE Select
|
ENSP00000315774.5:p.Tyr152Cys
|
|
ENST00000313468.9:c.455A>G
|
ENSP00000315774.5:p.Tyr152Cys
|
|
ENST00000524810.5:c.387A>G
|
|
|
ENST00000525419.5:c.401A>G
|
ENSP00000433521.1:p.Tyr134Cys
|
|
ENST00000526339.5:c.455A>G
|
ENSP00000436287.1:p.Tyr152Cys
|
|
ENST00000526446.5:c.*510A>G
|
ENSP00000433645.1:n.*510A>G
|
|
ENST00000528492.1:c.17A>G
|
ENSP00000432848.1:p.Tyr6Cys
|
|
ENST00000531282.1:n.307A>G
|
|
|
NM_002496.3:c.455A>G
|
NP_002487.1:p.Tyr152Cys
|
|
XM_005274013.1:c.455A>G
|
XP_005274070.1:p.Tyr152Cys
|
|
XM_005274014.1:c.455A>G
|
XP_005274071.1:p.Tyr152Cys
|
|
XM_005274015.1:c.335A>G
|
XP_005274072.1:p.Tyr112Cys
|
|
XM_011545053.1:c.455A>G
|
XP_011543355.1:p.Tyr152Cys
|
|
NM_002496.4:c.455A>G
MANE Select
|
NP_002487.1:p.Tyr152Cys
|
|