ENST00000456935.7:c.2090G>A
MANE Select
|
ENSP00000395473.2:p.Cys697Tyr
|
|
ENST00000221363.8:c.2087G>A
|
ENSP00000221363.4:p.Cys696Tyr
|
|
ENST00000456935.6:c.2090G>A
|
ENSP00000395473.2:p.Cys697Tyr
|
|
ENST00000466794.5:n.2680G>A
|
|
|
NM_000528.3:c.2090G>A
|
NP_000519.2:p.Cys697Tyr
|
|
NM_001173498.1:c.2087G>A
|
NP_001166969.1:p.Cys696Tyr
|
|
XM_005259913.1:c.2093G>A
|
XP_005259970.1:p.Cys698Tyr
|
|
XM_011528017.1:c.989G>A
|
XP_011526319.1:p.Cys330Tyr
|
|
XM_005259913.2:c.2093G>A
|
XP_005259970.1:p.Cys698Tyr
|
|
XM_024451518.1:c.989G>A
|
XP_024307286.1:p.Cys330Tyr
|
|
NM_000528.4:c.2090G>A
MANE Select
|
NP_000519.2:p.Cys697Tyr
|
|
NM_001173498.2:c.2087G>A
|
NP_001166969.1:p.Cys696Tyr
|
|