ENST00000350026.11:c.4897C>T
|
ENSP00000055163.8:p.Leu1633=
|
|
ENST00000414678.8:c.4966C>T
|
ENSP00000412835.3:p.Leu1656=
|
|
ENST00000637015.2:c.5185C>T
|
ENSP00000489729.2:p.Leu1729=
|
|
ENST00000346085.10:c.4936C>T
|
ENSP00000344546.5:p.Leu1646=
|
|
ENST00000350026.10:c.4648C>T
|
ENSP00000055163.7:p.Leu1550=
|
|
ENST00000414678.7:c.3214C>T
|
ENSP00000412835.2:p.Leu1072=
|
|
ENST00000635849.1:c.2377C>T
|
ENSP00000490948.1:p.Leu793=
|
|
ENST00000635957.1:c.2008C>T
|
ENSP00000490385.1:p.Leu670=
|
|
ENST00000636227.1:n.3519C>T
|
|
|
ENST00000636254.1:n.976C>T
|
|
|
ENST00000636930.2:c.5056C>T
MANE Select
|
ENSP00000490491.2:p.Leu1686=
|
|
ENST00000636940.1:n.3053C>T
|
|
|
ENST00000637015.1:c.2424C>T
|
|
|
ENST00000637568.1:c.2338C>T
|
|
|
ENST00000637741.1:n.1722C>T
|
|
|
ENST00000637810.1:c.2398C>T
|
ENSP00000489636.1:p.Leu800=
|
|
ENST00000637904.1:c.2557C>T
|
ENSP00000490550.1:p.Leu853=
|
|
ENST00000647938.1:c.4687C>T
|
ENSP00000498155.1:p.Leu1563=
|
|
ENST00000346085.9:c.4687C>T
|
ENSP00000344546.4:p.Leu1563=
|
|
ENST00000350026.9:c.4648C>T
|
ENSP00000055163.7:p.Leu1550=
|
|
ENST00000414678.6:c.3214C>T
|
ENSP00000412835.2:p.Leu1072=
|
|
NM_017519.2:c.4648C>T
|
NP_059989.2:p.Leu1550=
|
|
NM_020732.3:c.4687C>T
|
NP_065783.3:p.Leu1563=
|
|
XM_005267069.3:c.4807C>T
|
XP_005267126.2:p.Leu1603=
|
|
XM_011535984.1:c.3886C>T
|
XP_011534286.1:p.Leu1296=
|
|
XM_011535985.1:c.3706C>T
|
XP_011534287.1:p.Leu1236=
|
|
XM_011535986.1:c.3466C>T
|
XP_011534288.1:p.Leu1156=
|
|
XM_011535987.1:c.3085C>T
|
XP_011534289.1:p.Leu1029=
|
|
XM_011535988.1:c.1948C>T
|
XP_011534290.1:p.Leu650=
|
|
NM_001346813.1:c.4807C>T
|
NP_001333742.1:p.Leu1603=
|
|
NM_001363725.1:c.2557C>T
|
NP_001350654.1:p.Leu853=
|
|
XM_011535984.2:c.5017C>T
|
XP_011534286.2:p.Leu1673=
|
|
XM_011535988.3:c.1948C>T
|
XP_011534290.1:p.Leu650=
|
|
XM_017011103.2:c.4918C>T
|
XP_016866592.1:p.Leu1640=
|
|
XM_017011104.1:c.4888C>T
|
XP_016866593.1:p.Leu1630=
|
|
XM_017011105.2:c.4858C>T
|
XP_016866594.1:p.Leu1620=
|
|
XM_017011106.2:c.4729C>T
|
XP_016866595.1:p.Leu1577=
|
|
XM_017011107.2:c.4708C>T
|
XP_016866596.1:p.Leu1570=
|
|
XR_002956289.1:n.5003C>T
|
|
|
NM_001363725.2:c.2557C>T
|
NP_001350654.1:p.Leu853=
|
|
NM_001371656.1:c.4936C>T
|
NP_001358585.1:p.Leu1646=
|
|
NM_001374820.1:c.4936C>T
|
NP_001361749.1:p.Leu1646=
|
|
NM_001374828.1:c.5056C>T
MANE Select
|
NP_001361757.1:p.Leu1686=
|
|
NM_017519.3:c.4897C>T
|
NP_059989.3:p.Leu1633=
|
|