|
ENST00000418519.6:c.1019C=
MANE Select
|
ENSP00000415049.1:p.Ala340=
|
|
|
ENST00000309481.11:c.980C=
|
ENSP00000312584.7:p.Ala327=
|
|
|
ENST00000360317.7:c.1019C=
|
ENSP00000353465.3:p.Ala340=
|
|
|
ENST00000394175.6:c.953C=
|
ENSP00000377729.2:p.Ala318=
|
|
|
ENST00000394179.5:c.980C=
|
ENSP00000377733.2:p.Ala327=
|
|
|
ENST00000418519.5:c.1019C=
|
ENSP00000415049.1:p.Ala340=
|
|
|
ENST00000477054.6:n.4207C=
|
|
|
|
ENST00000479136.5:n.1760C=
|
|
|
|
ENST00000486560.1:n.84C=
|
|
|
|
ENST00000520542.5:c.992C=
|
ENSP00000430157.1:p.Ala331=
|
|
|
ENST00000522564.5:c.726C=
|
ENSP00000428217.1:n.726C=
|
|
|
ENST00000523371.5:c.895C=
|
ENSP00000429265.1:n.895C=
|
|
|
ENST00000524039.5:c.868C=
|
ENSP00000428712.1:n.868C=
|
|
|
NM_001042471.1:c.980C=
|
NP_001035936.1:p.Ala327=
|
|
|
NM_001165958.1:c.1019C=
|
NP_001159430.1:p.Ala340=
|
|
|
NM_001165959.1:c.992C=
|
NP_001159431.1:p.Ala331=
|
|
|
NM_018530.2:c.953C=
|
NP_061000.2:p.Ala318=
|
|
|
XM_011525001.1:c.1031C=
|
XP_011523303.1:p.Ala344=
|
|
|
XM_011525002.1:c.1031C=
|
XP_011523304.1:p.Ala344=
|
|
|
XM_011525003.1:c.1031C=
|
XP_011523305.1:p.Ala344=
|
|
|
XM_011525004.1:c.1031C=
|
XP_011523306.1:p.Ala344=
|
|
|
XM_011525005.1:c.1031C=
|
XP_011523307.1:p.Ala344=
|
|
|
XM_011525006.1:c.1031C=
|
XP_011523308.1:p.Ala344=
|
|
|
XM_011525007.1:c.1031C=
|
XP_011523309.1:p.Ala344=
|
|
|
XM_011525008.1:c.1031C=
|
XP_011523310.1:p.Ala344=
|
|
|
XM_011525009.1:c.1031C=
|
XP_011523311.1:p.Ala344=
|
|
|
XM_011525010.1:c.1031C=
|
XP_011523312.1:p.Ala344=
|
|
|
XM_011525011.1:c.1031C=
|
XP_011523313.1:p.Ala344=
|
|
|
XM_011525012.1:c.1031C=
|
XP_011523314.1:p.Ala344=
|
|
|
XM_011525013.1:c.1031C=
|
XP_011523315.1:p.Ala344=
|
|
|
XM_011525014.1:c.1031C=
|
XP_011523316.1:p.Ala344=
|
|
|
XM_011525015.1:c.1031C=
|
XP_011523317.1:p.Ala344=
|
|
|
XM_011525016.1:c.1019C=
|
XP_011523318.1:p.Ala340=
|
|
|
XM_011525017.1:c.1004C=
|
XP_011523319.1:p.Ala335=
|
|
|
XM_011525018.1:c.992C=
|
XP_011523320.1:p.Ala331=
|
|
|
XM_011525019.1:c.980C=
|
XP_011523321.1:p.Ala327=
|
|
|
XM_011525020.1:c.953C=
|
XP_011523322.1:p.Ala318=
|
|
|
XR_934504.1:n.2592C=
|
|
|
|
NM_001369402.1:c.980C=
|
NP_001356331.1:p.Ala327=
|
|
|
NM_001042471.2:c.980C=
|
NP_001035936.1:p.Ala327=
|
|
|
NM_001165958.2:c.1019C=
MANE Select
|
NP_001159430.1:p.Ala340=
|
|
|
NM_001165959.2:c.992C=
|
NP_001159431.1:p.Ala331=
|
|
|
NM_001369402.2:c.980C=
|
NP_001356331.1:p.Ala327=
|
|
|
NM_001388420.1:c.1019C=
|
NP_001375349.1:p.Ala340=
|
|
|
NM_001388421.1:c.992C=
|
NP_001375350.1:p.Ala331=
|
|
|
NM_001388422.1:c.980C=
|
NP_001375351.1:p.Ala327=
|
|
|
NM_001388423.1:c.953C=
|
NP_001375352.1:p.Ala318=
|
|
|
NM_001388424.1:c.707C=
|
NP_001375353.1:p.Ala236=
|
|
|
NM_018530.3:c.953C=
|
NP_061000.2:p.Ala318=
|
|
|
NR_170970.1:n.1113C=
|
|
|
|
NR_170971.1:n.2214C=
|
|
|
|
NR_170972.1:n.2130C=
|
|
|
|
NR_170973.1:n.2325C=
|
|
|
|
NR_170974.1:n.2187C=
|
|
|
