ENST00000683611.1:n.1178T>G
|
|
|
ENST00000265104.5:c.13845T>G
MANE Select
|
ENSP00000265104.4:p.Arg4615=
|
|
ENST00000681290.1:c.13800T>G
|
ENSP00000505288.1:p.Arg4600=
|
|
ENST00000265104.4:c.13845T>G
|
ENSP00000265104.4:p.Arg4615=
|
|
NM_001369.2:c.13845T>G
|
NP_001360.1:p.Arg4615=
|
|
XM_005248262.2:c.13800T>G
|
XP_005248319.1:p.Arg4600=
|
|
XM_005248262.3:c.13953T>G
|
XP_005248319.2:p.Arg4651=
|
|
XM_017009177.1:c.13533T>G
|
XP_016864666.1:p.Arg4511=
|
|
XM_017009178.1:c.12858T>G
|
XP_016864667.1:p.Arg4286=
|
|
XM_017009179.2:c.12858T>G
|
XP_016864668.1:p.Arg4286=
|
|
XM_017009185.1:c.9042T>G
|
XP_016864674.1:p.Arg3014=
|
|
XM_017009186.1:c.8595T>G
|
XP_016864675.1:p.Arg2865=
|
|
XM_017009188.1:c.7932T>G
|
XP_016864677.1:p.Arg2644=
|
|
XM_024454388.1:c.12858T>G
|
XP_024310156.1:p.Arg4286=
|
|
XM_024454389.1:c.12447T>G
|
XP_024310157.1:p.Arg4149=
|
|
NM_001369.3:c.13845T>G
MANE Select
|
NP_001360.1:p.Arg4615=
|
|