ENST00000685708.1:n.1388G>A
|
|
|
ENST00000685801.1:c.5018G>A
|
ENSP00000510688.1:p.Arg1673His
|
|
ENST00000691109.1:n.5250G>A
|
|
|
ENST00000216181.11:c.4955G>A
MANE Select
|
ENSP00000216181.6:p.Arg1652His
|
|
ENST00000216181.9:c.4955G>A
|
ENSP00000216181.5:p.Arg1652His
|
|
NM_002473.5:c.4955G>A , LRG_567t1:c.4955G>A
|
NP_002464.1:p.Arg1652His
|
|
XM_011530197.1:c.4955G>A
|
XP_011528499.1:p.Arg1652His
|
|
XM_011530197.2:c.4955G>A
|
XP_011528499.1:p.Arg1652His
|
|
XM_017028803.1:c.4955G>A
|
XP_016884292.1:p.Arg1652His
|
|
XM_017028804.1:c.4955G>A
|
XP_016884293.1:p.Arg1652His
|
|
XM_017028805.1:c.4955G>A
|
XP_016884294.1:p.Arg1652His
|
|
XM_017028806.1:c.4955G>A
|
XP_016884295.1:p.Arg1652His
|
|
NM_002473.6:c.4955G>A
MANE Select
|
NP_002464.1:p.Arg1652His
|
|