ENST00000378756.8:c.21T>A
MANE Select
|
ENSP00000368031.3:p.Ile7=
|
|
ENST00000672388.1:n.125T>A
|
|
|
ENST00000378755.9:c.21T>A
|
ENSP00000368030.5:p.Ile7=
|
|
ENST00000378756.7:c.21T>A
|
ENSP00000368031.3:p.Ile7=
|
|
NM_001170535.1:c.21T>A
|
NP_001164006.1:p.Ile7=
|
|
NM_018188.3:c.21T>A
|
NP_060658.3:p.Ile7=
|
|
NM_001170535.2:c.21T>A
|
NP_001164006.1:p.Ile7=
|
|
NM_018188.4:c.21T>A
|
NP_060658.3:p.Ile7=
|
|
XM_024448098.1:c.21T>A
|
XP_024303866.1:p.Ile7=
|
|
XR_001737282.1:n.147T>A
|
|
|
XR_002956997.1:n.147T>A
|
|
|
NM_001170535.3:c.21T>A
MANE Select
|
NP_001164006.1:p.Ile7=
|
|
NM_018188.5:c.21T>A
|
NP_060658.3:p.Ile7=
|
|