ENST00000683611.1:n.1096A>C
|
|
|
ENST00000265104.5:c.13763A>C
MANE Select
|
ENSP00000265104.4:p.Lys4588Thr
|
|
ENST00000681290.1:c.13718A>C
|
ENSP00000505288.1:p.Lys4573Thr
|
|
ENST00000265104.4:c.13763A>C
|
ENSP00000265104.4:p.Lys4588Thr
|
|
NM_001369.2:c.13763A>C
|
NP_001360.1:p.Lys4588Thr
|
|
XM_005248262.2:c.13718A>C
|
XP_005248319.1:p.Lys4573Thr
|
|
XM_005248262.3:c.13871A>C
|
XP_005248319.2:p.Lys4624Thr
|
|
XM_017009177.1:c.13451A>C
|
XP_016864666.1:p.Lys4484Thr
|
|
XM_017009178.1:c.12776A>C
|
XP_016864667.1:p.Lys4259Thr
|
|
XM_017009179.2:c.12776A>C
|
XP_016864668.1:p.Lys4259Thr
|
|
XM_017009185.1:c.8960A>C
|
XP_016864674.1:p.Lys2987Thr
|
|
XM_017009186.1:c.8513A>C
|
XP_016864675.1:p.Lys2838Thr
|
|
XM_017009188.1:c.7850A>C
|
XP_016864677.1:p.Lys2617Thr
|
|
XM_024454388.1:c.12776A>C
|
XP_024310156.1:p.Lys4259Thr
|
|
XM_024454389.1:c.12365A>C
|
XP_024310157.1:p.Lys4122Thr
|
|
NM_001369.3:c.13763A>C
MANE Select
|
NP_001360.1:p.Lys4588Thr
|
|