ENST00000683611.1:n.1108G>T
|
|
|
ENST00000265104.5:c.13775G>T
MANE Select
|
ENSP00000265104.4:p.Arg4592Leu
|
|
ENST00000681290.1:c.13730G>T
|
ENSP00000505288.1:p.Arg4577Leu
|
|
ENST00000265104.4:c.13775G>T
|
ENSP00000265104.4:p.Arg4592Leu
|
|
NM_001369.2:c.13775G>T
|
NP_001360.1:p.Arg4592Leu
|
|
XM_005248262.2:c.13730G>T
|
XP_005248319.1:p.Arg4577Leu
|
|
XM_005248262.3:c.13883G>T
|
XP_005248319.2:p.Arg4628Leu
|
|
XM_017009177.1:c.13463G>T
|
XP_016864666.1:p.Arg4488Leu
|
|
XM_017009178.1:c.12788G>T
|
XP_016864667.1:p.Arg4263Leu
|
|
XM_017009179.2:c.12788G>T
|
XP_016864668.1:p.Arg4263Leu
|
|
XM_017009185.1:c.8972G>T
|
XP_016864674.1:p.Arg2991Leu
|
|
XM_017009186.1:c.8525G>T
|
XP_016864675.1:p.Arg2842Leu
|
|
XM_017009188.1:c.7862G>T
|
XP_016864677.1:p.Arg2621Leu
|
|
XM_024454388.1:c.12788G>T
|
XP_024310156.1:p.Arg4263Leu
|
|
XM_024454389.1:c.12377G>T
|
XP_024310157.1:p.Arg4126Leu
|
|
NM_001369.3:c.13775G>T
MANE Select
|
NP_001360.1:p.Arg4592Leu
|
|