|
ENST00000412167.7:c.1923G>T
|
ENSP00000390987.3:p.Leu641=
|
|
|
ENST00000685269.1:n.2010G>T
|
|
|
|
ENST00000686011.1:c.1920G>T
|
ENSP00000509704.1:p.Leu640=
|
|
|
ENST00000687109.1:c.1935G>T
|
ENSP00000509371.1:p.Leu645=
|
|
|
ENST00000687208.1:n.2347G>T
|
|
|
|
ENST00000687246.1:c.1920G>T
|
ENSP00000509114.1:p.Leu640=
|
|
|
ENST00000687265.1:n.2090G>T
|
|
|
|
ENST00000687295.1:c.1920G>T
|
ENSP00000509450.1:p.Leu640=
|
|
|
ENST00000689832.1:c.1935G>T
|
ENSP00000509084.1:p.Leu645=
|
|
|
ENST00000689994.1:c.1422G>T
|
ENSP00000509156.1:p.Leu474=
|
|
|
ENST00000690543.1:c.1923G>T
|
ENSP00000508831.1:p.Leu641=
|
|
|
ENST00000690917.1:n.2150G>T
|
|
|
|
ENST00000691361.1:n.842G>T
|
|
|
|
ENST00000692783.1:c.1932G>T
|
ENSP00000508733.1:p.Leu644=
|
|
|
ENST00000692991.1:n.2029G>T
|
|
|
|
ENST00000288135.6:c.1932G>T
MANE Select
|
ENSP00000288135.6:p.Leu644=
|
|
|
ENST00000288135.5:c.1932G>T
|
ENSP00000288135.5:p.Leu644=
|
|
|
ENST00000412167.6:c.1920G>T
|
ENSP00000390987.2:p.Leu640=
|
|
|
NM_000222.2:c.1932G>T , LRG_307t1:c.1932G>T
|
NP_000213.1:p.Leu644=
|
|
|
NM_001093772.1:c.1920G>T
|
NP_001087241.1:p.Leu640=
|
|
|
XM_005265740.1:c.1935G>T
|
XP_005265797.1:p.Leu645=
|
|
|
XM_005265741.1:c.1935G>T
|
XP_005265798.1:p.Leu645=
|
|
|
XM_005265742.1:c.1923G>T
|
XP_005265799.1:p.Leu641=
|
|
|
XM_005265742.3:c.1923G>T
|
XP_005265799.1:p.Leu641=
|
|
|
XM_017008178.1:c.1932G>T
|
XP_016863667.1:p.Leu644=
|
|
|
XM_017008179.1:c.1923G>T
|
XP_016863668.1:p.Leu641=
|
|
|
XM_017008180.1:c.1920G>T
|
XP_016863669.1:p.Leu640=
|
|
|
NM_000222.3:c.1932G>T
MANE Select
|
NP_000213.1:p.Leu644=
|
|
|
NM_001093772.2:c.1920G>T
|
NP_001087241.1:p.Leu640=
|
|
|
NM_001385284.1:c.1935G>T
|
NP_001372213.1:p.Leu645=
|
|
|
NM_001385285.1:c.1932G>T
|
NP_001372214.1:p.Leu644=
|
|
|
NM_001385286.1:c.1920G>T
|
NP_001372215.1:p.Leu640=
|
|
|
NM_001385288.1:c.1923G>T
|
NP_001372217.1:p.Leu641=
|
|
|
NM_001385290.1:c.1935G>T
|
NP_001372219.1:p.Leu645=
|
|
|
NM_001385292.1:c.1923G>T
|
NP_001372221.1:p.Leu641=
|
|
