ENST00000371117.8:c.11707C>T
MANE Select
|
ENSP00000360158.3:p.Gln3903Ter
|
|
ENST00000371117.7:c.11707C>T
|
ENSP00000360158.3:p.Gln3903Ter
|
|
NM_138694.3:c.11707C>T
|
NP_619639.3:p.Gln3903Ter
|
|
XM_011514679.1:c.11707C>T
|
XP_011512981.1:p.Gln3903Ter
|
|
XM_011514680.1:c.11707C>T
|
XP_011512982.1:p.Gln3903Ter
|
|
XM_011514681.1:c.11578C>T
|
XP_011512983.1:p.Gln3860Ter
|
|
XM_011514682.1:c.11569C>T
|
XP_011512984.1:p.Gln3857Ter
|
|
XM_011514683.1:c.11065C>T
|
XP_011512985.1:p.Gln3689Ter
|
|
XM_011514684.1:c.10996C>T
|
XP_011512986.1:p.Gln3666Ter
|
|
XM_011514690.1:c.5782C>T
|
XP_011512992.1:p.Gln1928Ter
|
|
XM_011514691.1:c.5782C>T
|
XP_011512993.1:p.Gln1928Ter
|
|
XM_011514680.3:c.11707C>T
|
XP_011512982.1:p.Gln3903Ter
|
|
XM_011514682.3:c.11569C>T
|
XP_011512984.1:p.Gln3857Ter
|
|
XM_011514683.3:c.11065C>T
|
XP_011512985.1:p.Gln3689Ter
|
|
XM_011514684.3:c.10996C>T
|
XP_011512986.1:p.Gln3666Ter
|
|
XM_011514690.3:c.5782C>T
|
XP_011512992.1:p.Gln1928Ter
|
|
XM_011514691.3:c.5782C>T
|
XP_011512993.1:p.Gln1928Ter
|
|
XM_017010944.2:c.11707C>T
|
XP_016866433.1:p.Gln3903Ter
|
|
XM_017010945.2:c.11632C>T
|
XP_016866434.1:p.Gln3878Ter
|
|
XM_017010946.2:c.11512C>T
|
XP_016866435.1:p.Gln3838Ter
|
|
XM_017010947.2:c.11443C>T
|
XP_016866436.1:p.Gln3815Ter
|
|
XM_017010948.2:c.10996C>T
|
XP_016866437.1:p.Gln3666Ter
|
|
XM_017010949.2:c.9847C>T
|
XP_016866438.1:p.Gln3283Ter
|
|
NM_138694.4:c.11707C>T
MANE Select
|
NP_619639.3:p.Gln3903Ter
|
|