ENST00000261978.9:c.5411G>A
MANE Select
|
ENSP00000261978.4:p.Cys1804Tyr
|
|
ENST00000261978.8:c.5411G>A
|
ENSP00000261978.4:p.Cys1804Tyr
|
|
ENST00000553939.5:c.*190G>A
|
ENSP00000452110.1:n.*190G>A
|
|
ENST00000554861.1:n.629G>A
|
|
|
ENST00000556690.5:c.5279G>A
|
ENSP00000451477.1:p.Cys1760Tyr
|
|
NM_000428.2:c.5411G>A
|
NP_000419.1:p.Cys1804Tyr
|
|
XM_011536765.1:c.5030G>A
|
XP_011535067.1:p.Cys1677Tyr
|
|
XM_011536766.1:c.4952G>A
|
XP_011535068.1:p.Cys1651Tyr
|
|
XM_011536767.1:c.4928G>A
|
XP_011535069.1:p.Cys1643Tyr
|
|
XM_011536765.2:c.5030G>A
|
XP_011535067.1:p.Cys1677Tyr
|
|
NM_000428.3:c.5411G>A
MANE Select
|
NP_000419.1:p.Cys1804Tyr
|
|