ENST00000683611.1:n.1072G>T
|
|
|
ENST00000265104.5:c.13739G>T
MANE Select
|
ENSP00000265104.4:p.Arg4580Leu
|
|
ENST00000681290.1:c.13694G>T
|
ENSP00000505288.1:p.Arg4565Leu
|
|
ENST00000265104.4:c.13739G>T
|
ENSP00000265104.4:p.Arg4580Leu
|
|
NM_001369.2:c.13739G>T
|
NP_001360.1:p.Arg4580Leu
|
|
XM_005248262.2:c.13694G>T
|
XP_005248319.1:p.Arg4565Leu
|
|
XM_005248262.3:c.13847G>T
|
XP_005248319.2:p.Arg4616Leu
|
|
XM_017009177.1:c.13427G>T
|
XP_016864666.1:p.Arg4476Leu
|
|
XM_017009178.1:c.12752G>T
|
XP_016864667.1:p.Arg4251Leu
|
|
XM_017009179.2:c.12752G>T
|
XP_016864668.1:p.Arg4251Leu
|
|
XM_017009185.1:c.8936G>T
|
XP_016864674.1:p.Arg2979Leu
|
|
XM_017009186.1:c.8489G>T
|
XP_016864675.1:p.Arg2830Leu
|
|
XM_017009188.1:c.7826G>T
|
XP_016864677.1:p.Arg2609Leu
|
|
XM_024454388.1:c.12752G>T
|
XP_024310156.1:p.Arg4251Leu
|
|
XM_024454389.1:c.12341G>T
|
XP_024310157.1:p.Arg4114Leu
|
|
NM_001369.3:c.13739G>T
MANE Select
|
NP_001360.1:p.Arg4580Leu
|
|