ENST00000685708.1:n.1999A>C
|
|
|
ENST00000685801.1:c.5629A>C
|
ENSP00000510688.1:p.Arg1877=
|
|
ENST00000690244.1:n.902A>C
|
|
|
ENST00000691109.1:n.5861A>C
|
|
|
ENST00000216181.11:c.5566A>C
MANE Select
|
ENSP00000216181.6:p.Arg1856=
|
|
ENST00000216181.9:c.5566A>C
|
ENSP00000216181.5:p.Arg1856=
|
|
ENST00000475726.5:n.596A>C
|
|
|
ENST00000486218.1:n.573A>C
|
|
|
NM_002473.5:c.5566A>C , LRG_567t1:c.5566A>C
|
NP_002464.1:p.Arg1856=
|
|
XM_011530197.1:c.5566A>C
|
XP_011528499.1:p.Arg1856=
|
|
XM_011530197.2:c.5566A>C
|
XP_011528499.1:p.Arg1856=
|
|
XM_017028803.1:c.5566A>C
|
XP_016884292.1:p.Arg1856=
|
|
XM_017028804.1:c.5566A>C
|
XP_016884293.1:p.Arg1856=
|
|
XM_017028805.1:c.5566A>C
|
XP_016884294.1:p.Arg1856=
|
|
XM_017028806.1:c.5566A>C
|
XP_016884295.1:p.Arg1856=
|
|
NM_002473.6:c.5566A>C
MANE Select
|
NP_002464.1:p.Arg1856=
|
|