ENST00000371117.8:c.8976A>G
MANE Select
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ENSP00000360158.3:p.Glu2992=
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ENST00000340994.4:c.8976A>G
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ENSP00000341097.4:p.Glu2992=
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|
ENST00000371117.7:c.8976A>G
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ENSP00000360158.3:p.Glu2992=
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|
NM_138694.3:c.8976A>G
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NP_619639.3:p.Glu2992=
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|
NM_170724.2:c.8976A>G
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NP_733842.2:p.Glu2992=
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|
XM_011514679.1:c.8976A>G
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XP_011512981.1:p.Glu2992=
|
|
XM_011514680.1:c.8976A>G
|
XP_011512982.1:p.Glu2992=
|
|
XM_011514681.1:c.8847A>G
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XP_011512983.1:p.Glu2949=
|
|
XM_011514682.1:c.8838A>G
|
XP_011512984.1:p.Glu2946=
|
|
XM_011514683.1:c.8334A>G
|
XP_011512985.1:p.Glu2778=
|
|
XM_011514684.1:c.8265A>G
|
XP_011512986.1:p.Glu2755=
|
|
XM_011514685.1:c.8976A>G
|
XP_011512987.1:p.Glu2992=
|
|
XM_011514686.1:c.8976A>G
|
XP_011512988.1:p.Glu2992=
|
|
XM_011514687.1:c.8976A>G
|
XP_011512989.1:p.Glu2992=
|
|
XM_011514688.1:c.8976A>G
|
XP_011512990.1:p.Glu2992=
|
|
XM_011514690.1:c.3051A>G
|
XP_011512992.1:p.Glu1017=
|
|
XM_011514691.1:c.3051A>G
|
XP_011512993.1:p.Glu1017=
|
|
XM_011514680.3:c.8976A>G
|
XP_011512982.1:p.Glu2992=
|
|
XM_011514682.3:c.8838A>G
|
XP_011512984.1:p.Glu2946=
|
|
XM_011514683.3:c.8334A>G
|
XP_011512985.1:p.Glu2778=
|
|
XM_011514684.3:c.8265A>G
|
XP_011512986.1:p.Glu2755=
|
|
XM_011514686.2:c.8976A>G
|
XP_011512988.1:p.Glu2992=
|
|
XM_011514688.2:c.8976A>G
|
XP_011512990.1:p.Glu2992=
|
|
XM_011514690.3:c.3051A>G
|
XP_011512992.1:p.Glu1017=
|
|
XM_011514691.3:c.3051A>G
|
XP_011512993.1:p.Glu1017=
|
|
XM_017010944.2:c.8976A>G
|
XP_016866433.1:p.Glu2992=
|
|
XM_017010945.2:c.8901A>G
|
XP_016866434.1:p.Glu2967=
|
|
XM_017010946.2:c.8781A>G
|
XP_016866435.1:p.Glu2927=
|
|
XM_017010947.2:c.8712A>G
|
XP_016866436.1:p.Glu2904=
|
|
XM_017010948.2:c.8265A>G
|
XP_016866437.1:p.Glu2755=
|
|
XM_017010949.2:c.7116A>G
|
XP_016866438.1:p.Glu2372=
|
|
XM_017010950.1:c.8976A>G
|
XP_016866439.1:p.Glu2992=
|
|
XR_001743469.1:n.9252A>G
|
|
|
NM_138694.4:c.8976A>G
MANE Select
|
NP_619639.3:p.Glu2992=
|
|
NM_170724.3:c.8976A>G
|
NP_733842.2:p.Glu2992=
|
|