ENST00000371117.8:c.8822G>A
MANE Select
|
ENSP00000360158.3:p.Gly2941Asp
|
|
ENST00000340994.4:c.8822G>A
|
ENSP00000341097.4:p.Gly2941Asp
|
|
ENST00000371117.7:c.8822G>A
|
ENSP00000360158.3:p.Gly2941Asp
|
|
NM_138694.3:c.8822G>A
|
NP_619639.3:p.Gly2941Asp
|
|
NM_170724.2:c.8822G>A
|
NP_733842.2:p.Gly2941Asp
|
|
XM_011514679.1:c.8822G>A
|
XP_011512981.1:p.Gly2941Asp
|
|
XM_011514680.1:c.8822G>A
|
XP_011512982.1:p.Gly2941Asp
|
|
XM_011514681.1:c.8693G>A
|
XP_011512983.1:p.Gly2898Asp
|
|
XM_011514682.1:c.8684G>A
|
XP_011512984.1:p.Gly2895Asp
|
|
XM_011514683.1:c.8180G>A
|
XP_011512985.1:p.Gly2727Asp
|
|
XM_011514684.1:c.8111G>A
|
XP_011512986.1:p.Gly2704Asp
|
|
XM_011514685.1:c.8822G>A
|
XP_011512987.1:p.Gly2941Asp
|
|
XM_011514686.1:c.8822G>A
|
XP_011512988.1:p.Gly2941Asp
|
|
XM_011514687.1:c.8822G>A
|
XP_011512989.1:p.Gly2941Asp
|
|
XM_011514688.1:c.8822G>A
|
XP_011512990.1:p.Gly2941Asp
|
|
XM_011514690.1:c.2897G>A
|
XP_011512992.1:p.Gly966Asp
|
|
XM_011514691.1:c.2897G>A
|
XP_011512993.1:p.Gly966Asp
|
|
XM_011514680.3:c.8822G>A
|
XP_011512982.1:p.Gly2941Asp
|
|
XM_011514682.3:c.8684G>A
|
XP_011512984.1:p.Gly2895Asp
|
|
XM_011514683.3:c.8180G>A
|
XP_011512985.1:p.Gly2727Asp
|
|
XM_011514684.3:c.8111G>A
|
XP_011512986.1:p.Gly2704Asp
|
|
XM_011514686.2:c.8822G>A
|
XP_011512988.1:p.Gly2941Asp
|
|
XM_011514688.2:c.8822G>A
|
XP_011512990.1:p.Gly2941Asp
|
|
XM_011514690.3:c.2897G>A
|
XP_011512992.1:p.Gly966Asp
|
|
XM_011514691.3:c.2897G>A
|
XP_011512993.1:p.Gly966Asp
|
|
XM_017010944.2:c.8822G>A
|
XP_016866433.1:p.Gly2941Asp
|
|
XM_017010945.2:c.8747G>A
|
XP_016866434.1:p.Gly2916Asp
|
|
XM_017010946.2:c.8627G>A
|
XP_016866435.1:p.Gly2876Asp
|
|
XM_017010947.2:c.8558G>A
|
XP_016866436.1:p.Gly2853Asp
|
|
XM_017010948.2:c.8111G>A
|
XP_016866437.1:p.Gly2704Asp
|
|
XM_017010949.2:c.6962G>A
|
XP_016866438.1:p.Gly2321Asp
|
|
XM_017010950.1:c.8822G>A
|
XP_016866439.1:p.Gly2941Asp
|
|
XM_017010951.1:c.*1426G>A
|
XP_016866440.1:n.*1426G>A
|
|
XR_001743469.1:n.9098G>A
|
|
|
NM_138694.4:c.8822G>A
MANE Select
|
NP_619639.3:p.Gly2941Asp
|
|
NM_170724.3:c.8822G>A
|
NP_733842.2:p.Gly2941Asp
|
|