ENST00000510830.2:n.1882A>C
|
|
|
ENST00000651892.2:c.8883A>C
MANE Select
|
ENSP00000498265.2:p.Arg2961Ser
|
|
ENST00000676160.1:n.744A>C
|
|
|
ENST00000425232.6:c.8721A>C
|
ENSP00000389014.2:p.Arg2907Ser
|
|
ENST00000508244.5:c.8721A>C
|
ENSP00000421690.1:p.Arg2907Ser
|
|
ENST00000509849.5:c.5895A>C
|
ENSP00000426337.1:n.5895A>C
|
|
ENST00000509957.5:n.4064A>C
|
|
|
ENST00000512288.5:n.342-3535A>C
|
|
|
ENST00000514429.5:c.5919A>C
|
ENSP00000424223.1:p.Arg1973Ser
|
|
NM_023073.3:c.8721A>C
|
NP_075561.3:p.Arg2907Ser
|
|
XM_005248345.2:c.8883A>C
|
XP_005248402.1:p.Arg2961Ser
|
|
XM_005248346.2:c.8880A>C
|
XP_005248403.1:p.Arg2960Ser
|
|
XM_005248347.2:c.8880A>C
|
XP_005248404.1:p.Arg2960Ser
|
|
XM_005248349.2:c.8772A>C
|
XP_005248406.1:p.Arg2924Ser
|
|
XM_005248350.2:c.8754A>C
|
XP_005248407.1:p.Arg2918Ser
|
|
XM_005248353.3:c.5526A>C
|
XP_005248410.1:p.Arg1842Ser
|
|
XM_006714489.2:c.8883A>C
|
XP_006714552.1:p.Arg2961Ser
|
|
XM_006714491.2:c.3456A>C
|
XP_006714554.1:p.Arg1152Ser
|
|
XM_011514085.1:c.8883A>C
|
XP_011512387.1:p.Arg2961Ser
|
|
XM_011514086.1:c.8883A>C
|
XP_011512388.1:p.Arg2961Ser
|
|
XM_011514087.1:c.8829A>C
|
XP_011512389.1:p.Arg2943Ser
|
|
XM_011514088.1:c.8775A>C
|
XP_011512390.1:p.Arg2925Ser
|
|
XM_011514089.1:c.8883A>C
|
XP_011512391.1:p.Arg2961Ser
|
|
XM_011514090.1:c.8565A>C
|
XP_011512392.1:p.Arg2855Ser
|
|
XM_011514091.1:c.8211A>C
|
XP_011512393.1:p.Arg2737Ser
|
|
XM_011514092.1:c.8883A>C
|
XP_011512394.1:p.Arg2961Ser
|
|
XM_011514094.1:c.6108A>C
|
XP_011512396.1:p.Arg2036Ser
|
|
XR_427661.2:n.9058A>C
|
|
|
XR_925644.1:n.9058A>C
|
|
|
XM_005248345.4:c.8883A>C
|
XP_005248402.1:p.Arg2961Ser
|
|
XM_005248346.4:c.8880A>C
|
XP_005248403.1:p.Arg2960Ser
|
|
XM_005248347.4:c.8880A>C
|
XP_005248404.1:p.Arg2960Ser
|
|
XM_005248349.4:c.8772A>C
|
XP_005248406.1:p.Arg2924Ser
|
|
XM_005248350.4:c.8754A>C
|
XP_005248407.1:p.Arg2918Ser
|
|
XM_006714491.3:c.3456A>C
|
XP_006714554.1:p.Arg1152Ser
|
|
XM_011514085.3:c.8883A>C
|
XP_011512387.1:p.Arg2961Ser
|
|
XM_011514086.3:c.8883A>C
|
XP_011512388.1:p.Arg2961Ser
|
|
XM_011514087.2:c.8829A>C
|
XP_011512389.1:p.Arg2943Ser
|
|
XM_011514088.2:c.8775A>C
|
XP_011512390.1:p.Arg2925Ser
|
|
XM_011514089.2:c.8883A>C
|
XP_011512391.1:p.Arg2961Ser
|
|
XM_011514090.3:c.8565A>C
|
XP_011512392.1:p.Arg2855Ser
|
|
XM_011514092.2:c.8883A>C
|
XP_011512394.1:p.Arg2961Ser
|
|
XM_011514094.2:c.6108A>C
|
XP_011512396.1:p.Arg2036Ser
|
|
XM_017009760.1:c.8694A>C
|
XP_016865249.1:p.Arg2898Ser
|
|
XM_017009761.2:c.8694A>C
|
XP_016865250.1:p.Arg2898Ser
|
|
XM_017009763.1:c.7890A>C
|
XP_016865252.1:p.Arg2630Ser
|
|
XM_017009765.1:c.7695A>C
|
XP_016865254.1:p.Arg2565Ser
|
|
XM_017009766.1:c.5526A>C
|
XP_016865255.1:p.Arg1842Ser
|
|
XM_024446183.1:c.8694A>C
|
XP_024301951.1:p.Arg2898Ser
|
|
XM_024446184.1:c.8565A>C
|
XP_024301952.1:p.Arg2855Ser
|
|
XM_024446185.1:c.8211A>C
|
XP_024301953.1:p.Arg2737Ser
|
|
XM_024446186.1:c.7890A>C
|
XP_024301954.1:p.Arg2630Ser
|
|
XR_925644.2:n.9107A>C
|
|
|
NM_001384732.1:c.8883A>C
MANE Select
|
NP_001371661.1:p.Arg2961Ser
|
|
NM_023073.4:c.8721A>C
|
NP_075561.3:p.Arg2907Ser
|
|