ENST00000456935.7:c.2742G>T
MANE Select
|
ENSP00000395473.2:p.Leu914=
|
|
ENST00000221363.8:c.2739G>T
|
ENSP00000221363.4:p.Leu913=
|
|
ENST00000456935.6:c.2742G>T
|
ENSP00000395473.2:p.Leu914=
|
|
ENST00000466794.5:n.3332G>T
|
|
|
ENST00000469423.1:n.64G>T
|
|
|
ENST00000493218.5:n.153G>T
|
|
|
ENST00000597692.1:c.301G>T
|
|
|
NM_000528.3:c.2742G>T
|
NP_000519.2:p.Leu914=
|
|
NM_001173498.1:c.2739G>T
|
NP_001166969.1:p.Leu913=
|
|
XM_005259913.1:c.2745G>T
|
XP_005259970.1:p.Leu915=
|
|
XM_011528017.1:c.1641G>T
|
XP_011526319.1:p.Leu547=
|
|
XM_005259913.2:c.2745G>T
|
XP_005259970.1:p.Leu915=
|
|
XM_024451518.1:c.1641G>T
|
XP_024307286.1:p.Leu547=
|
|
NM_000528.4:c.2742G>T
MANE Select
|
NP_000519.2:p.Leu914=
|
|
NM_001173498.2:c.2739G>T
|
NP_001166969.1:p.Leu913=
|
|