ENST00000360256.9:c.6876_6878delinsCTT
MANE Select
|
ENSP00000353393.4:p.Leu2292=
|
|
ENST00000644698.1:c.609_611delinsCTT
|
ENSP00000495706.1:p.Leu203=
|
|
ENST00000330287.10:c.471_473delinsCTT
|
ENSP00000327895.6:p.Leu157=
|
|
ENST00000360256.8:c.6876_6878delinsCTT
|
ENSP00000353393.4:p.Leu2292=
|
|
NM_000132.3:c.6876_6878delinsCTT
|
NP_000123.1:p.Leu2292=
|
|
NM_019863.2:c.471_473delinsCTT
|
NP_063916.1:p.Leu157=
|
|
XM_011531126.1:c.6771_6773delinsCTT
|
XP_011529428.1:p.Leu2257=
|
|
NM_000132.4:c.6876_6878delinsCTT
MANE Select
|
NP_000123.1:p.Leu2292=
|
|
NM_019863.3:c.471_473delinsCTT
|
NP_063916.1:p.Leu157=
|
|