|
ENST00000581113.7:c.1971A>T
|
ENSP00000492721.2:n.1971A>T
|
|
|
ENST00000696138.1:c.5765A>T
|
ENSP00000512431.1:p.Glu1922Val
|
|
|
ENST00000684826.1:c.347A>T
|
ENSP00000509994.1:p.Glu116Val
|
|
|
ENST00000687027.1:c.-62A>T
|
ENSP00000508715.1:n.-62A>T
|
|
|
ENST00000687863.1:n.2428A>T
|
|
|
|
ENST00000691014.1:c.5813A>T
|
ENSP00000510595.1:p.Glu1938Val
|
|
|
ENST00000693617.1:c.347A>T
|
ENSP00000510031.1:p.Glu116Val
|
|
|
ENST00000358273.9:c.5783A>T
MANE Select
|
ENSP00000351015.4:p.Glu1928Val
|
|
|
ENST00000356175.7:c.5720A>T
|
ENSP00000348498.3:p.Glu1907Val
|
|
|
ENST00000358273.8:c.5783A>T
|
ENSP00000351015.4:p.Glu1928Val
|
|
|
ENST00000456735.6:c.4718A>T
|
ENSP00000389907.2:p.Glu1573Val
|
|
|
ENST00000479536.2:c.141A>T
|
|
|
|
ENST00000493220.5:n.4256A>T
|
|
|
|
ENST00000579081.5:c.5919A>T
|
ENSP00000462408.1:n.5919A>T
|
|
|
ENST00000581113.6:n.1100A>T
|
|
|
|
NM_000267.3:c.5720A>T , LRG_214t1:c.5720A>T
|
NP_000258.1:p.Glu1907Val
|
|
|
NM_001042492.2:c.5783A>T , LRG_214t2:c.5783A>T
|
NP_001035957.1:p.Glu1928Val
|
|
|
XM_005257983.1:c.5783A>T
|
XP_005258040.1:p.Glu1928Val
|
|
|
XM_005257984.1:c.5720A>T
|
XP_005258041.1:p.Glu1907Val
|
|
|
XM_006721922.1:c.5813A>T
|
XP_006721985.1:p.Glu1938Val
|
|
|
XM_006721923.2:c.5774A>T
|
XP_006721986.1:p.Glu1925Val
|
|
|
XM_006721924.1:c.5813A>T
|
XP_006721987.1:p.Glu1938Val
|
|
|
XM_006721925.1:c.5750A>T
|
XP_006721988.1:p.Glu1917Val
|
|
|
XM_006721926.2:c.5813A>T
|
XP_006721989.1:p.Glu1938Val
|
|
|
XM_006721927.1:c.5813A>T
|
XP_006721990.1:p.Glu1938Val
|
|
|
XM_011524852.1:c.5810A>T
|
XP_011523154.1:p.Glu1937Val
|
|
|
XM_011524853.1:c.5774A>T
|
XP_011523155.1:p.Glu1925Val
|
|
|
XM_011524854.1:c.5774A>T
|
XP_011523156.1:p.Glu1925Val
|
|
|
XM_011524855.1:c.5774A>T
|
XP_011523157.1:p.Glu1925Val
|
|
|
XM_011524856.1:c.5774A>T
|
XP_011523158.1:p.Glu1925Val
|
|
|
XM_011524857.1:c.5813A>T
|
XP_011523159.1:p.Glu1938Val
|
|
|
NM_001042492.3:c.5783A>T
MANE Select
|
NP_001035957.1:p.Glu1928Val
|
|
