ENST00000376215.10:c.12C>T
MANE Select
|
ENSP00000365388.5:p.Arg4=
|
|
ENST00000376215.9:c.12C>T
|
ENSP00000365388.5:p.Arg4=
|
|
NM_014317.3:c.12C>T
|
NP_055132.2:p.Arg4=
|
|
XR_428636.2:n.300C>T
|
|
|
XR_930486.1:n.300C>T
|
|
|
NM_001321978.1:c.12C>T
|
NP_001308907.1:p.Arg4=
|
|
NM_001321979.1:c.-582C>T
|
NP_001308908.1:n.-582C>T
|
|
NM_014317.4:c.12C>T
|
NP_055132.2:p.Arg4=
|
|
XM_024447922.1:c.12C>T
|
XP_024303690.1:p.Arg4=
|
|
XR_428636.4:n.300C>T
|
|
|
NM_014317.5:c.12C>T
MANE Select
|
NP_055132.2:p.Arg4=
|
|
NM_001321978.2:c.12C>T
|
NP_001308907.1:p.Arg4=
|
|
NM_001321979.2:c.-582C>T
|
NP_001308908.1:n.-582C>T
|
|