ENST00000371117.8:c.10228C>T
MANE Select
|
ENSP00000360158.3:p.Gln3410Ter
|
|
ENST00000371117.7:c.10228C>T
|
ENSP00000360158.3:p.Gln3410Ter
|
|
NM_138694.3:c.10228C>T
|
NP_619639.3:p.Gln3410Ter
|
|
XM_011514679.1:c.10228C>T
|
XP_011512981.1:p.Gln3410Ter
|
|
XM_011514680.1:c.10228C>T
|
XP_011512982.1:p.Gln3410Ter
|
|
XM_011514681.1:c.10099C>T
|
XP_011512983.1:p.Gln3367Ter
|
|
XM_011514682.1:c.10090C>T
|
XP_011512984.1:p.Gln3364Ter
|
|
XM_011514683.1:c.9586C>T
|
XP_011512985.1:p.Gln3196Ter
|
|
XM_011514684.1:c.9517C>T
|
XP_011512986.1:p.Gln3173Ter
|
|
XM_011514687.1:c.10157-10678C>T
|
XP_011512989.1:n.10157-10678C>T
|
|
XM_011514690.1:c.4303C>T
|
XP_011512992.1:p.Gln1435Ter
|
|
XM_011514691.1:c.4303C>T
|
XP_011512993.1:p.Gln1435Ter
|
|
XR_926870.1:n.535+7525G>A
|
|
|
XR_926871.1:n.403+7525G>A
|
|
|
XR_926872.1:n.535+7525G>A
|
|
|
XM_011514680.3:c.10228C>T
|
XP_011512982.1:p.Gln3410Ter
|
|
XM_011514682.3:c.10090C>T
|
XP_011512984.1:p.Gln3364Ter
|
|
XM_011514683.3:c.9586C>T
|
XP_011512985.1:p.Gln3196Ter
|
|
XM_011514684.3:c.9517C>T
|
XP_011512986.1:p.Gln3173Ter
|
|
XM_011514690.3:c.4303C>T
|
XP_011512992.1:p.Gln1435Ter
|
|
XM_011514691.3:c.4303C>T
|
XP_011512993.1:p.Gln1435Ter
|
|
XM_017010944.2:c.10228C>T
|
XP_016866433.1:p.Gln3410Ter
|
|
XM_017010945.2:c.10153C>T
|
XP_016866434.1:p.Gln3385Ter
|
|
XM_017010946.2:c.10033C>T
|
XP_016866435.1:p.Gln3345Ter
|
|
XM_017010947.2:c.9964C>T
|
XP_016866436.1:p.Gln3322Ter
|
|
XM_017010948.2:c.9517C>T
|
XP_016866437.1:p.Gln3173Ter
|
|
XM_017010949.2:c.8368C>T
|
XP_016866438.1:p.Gln2790Ter
|
|
XR_001743469.1:n.10504C>T
|
|
|
XR_001744157.1:n.3145+7525G>A
|
|
|
XR_926870.2:n.3145+7525G>A
|
|
|
XR_926871.2:n.3013+7525G>A
|
|
|
XR_926872.2:n.3145+7525G>A
|
|
|
NM_138694.4:c.10228C>T
MANE Select
|
NP_619639.3:p.Gln3410Ter
|
|