ENST00000233190.11:c.828T>A
MANE Select
|
ENSP00000233190.5:p.Arg276=
|
|
ENST00000233190.10:c.828T>A
|
ENSP00000233190.5:p.Arg276=
|
|
ENST00000423725.5:c.657T>A
|
ENSP00000397760.1:p.Arg219=
|
|
ENST00000432169.5:c.495T>A
|
ENSP00000409689.1:p.Arg165=
|
|
ENST00000440274.5:c.720T>A
|
ENSP00000409766.1:p.Arg240=
|
|
ENST00000449699.5:c.828T>A
|
ENSP00000399912.1:p.Arg276=
|
|
ENST00000455934.6:c.870T>A
|
ENSP00000392709.2:p.Arg290=
|
|
ENST00000457011.5:c.480T>A
|
ENSP00000400976.1:p.Arg160=
|
|
NM_001199981.1:c.720T>A
|
NP_001186910.1:p.Arg240=
|
|
NM_001199982.1:c.495T>A
|
NP_001186911.1:p.Arg165=
|
|
NM_001199983.1:c.657T>A
|
NP_001186912.1:p.Arg219=
|
|
NM_001199984.1:c.870T>A
|
NP_001186913.1:p.Arg290=
|
|
NM_005006.6:c.828T>A
|
NP_004997.4:p.Arg276=
|
|
XM_017004188.2:c.69T>A
|
XP_016859677.1:p.Arg23=
|
|
NM_001199981.2:c.720T>A
|
NP_001186910.1:p.Arg240=
|
|
NM_001199982.2:c.495T>A
|
NP_001186911.1:p.Arg165=
|
|
NM_001199983.2:c.657T>A
|
NP_001186912.1:p.Arg219=
|
|
NM_005006.7:c.828T>A
MANE Select
|
NP_004997.4:p.Arg276=
|
|
NM_001199984.2:c.870T>A
|
NP_001186913.1:p.Arg290=
|
|