ENST00000683611.1:n.1145G>C
|
|
|
ENST00000265104.5:c.13812G>C
MANE Select
|
ENSP00000265104.4:p.Arg4604Ser
|
|
ENST00000681290.1:c.13767G>C
|
ENSP00000505288.1:p.Arg4589Ser
|
|
ENST00000265104.4:c.13812G>C
|
ENSP00000265104.4:p.Arg4604Ser
|
|
NM_001369.2:c.13812G>C
|
NP_001360.1:p.Arg4604Ser
|
|
XM_005248262.2:c.13767G>C
|
XP_005248319.1:p.Arg4589Ser
|
|
XM_005248262.3:c.13920G>C
|
XP_005248319.2:p.Arg4640Ser
|
|
XM_017009177.1:c.13500G>C
|
XP_016864666.1:p.Arg4500Ser
|
|
XM_017009178.1:c.12825G>C
|
XP_016864667.1:p.Arg4275Ser
|
|
XM_017009179.2:c.12825G>C
|
XP_016864668.1:p.Arg4275Ser
|
|
XM_017009185.1:c.9009G>C
|
XP_016864674.1:p.Arg3003Ser
|
|
XM_017009186.1:c.8562G>C
|
XP_016864675.1:p.Arg2854Ser
|
|
XM_017009188.1:c.7899G>C
|
XP_016864677.1:p.Arg2633Ser
|
|
XM_024454388.1:c.12825G>C
|
XP_024310156.1:p.Arg4275Ser
|
|
XM_024454389.1:c.12414G>C
|
XP_024310157.1:p.Arg4138Ser
|
|
NM_001369.3:c.13812G>C
MANE Select
|
NP_001360.1:p.Arg4604Ser
|
|