ENST00000683611.1:n.1111C>A
|
|
|
ENST00000265104.5:c.13778C>A
MANE Select
|
ENSP00000265104.4:p.Thr4593Lys
|
|
ENST00000681290.1:c.13733C>A
|
ENSP00000505288.1:p.Thr4578Lys
|
|
ENST00000265104.4:c.13778C>A
|
ENSP00000265104.4:p.Thr4593Lys
|
|
NM_001369.2:c.13778C>A
|
NP_001360.1:p.Thr4593Lys
|
|
XM_005248262.2:c.13733C>A
|
XP_005248319.1:p.Thr4578Lys
|
|
XM_005248262.3:c.13886C>A
|
XP_005248319.2:p.Thr4629Lys
|
|
XM_017009177.1:c.13466C>A
|
XP_016864666.1:p.Thr4489Lys
|
|
XM_017009178.1:c.12791C>A
|
XP_016864667.1:p.Thr4264Lys
|
|
XM_017009179.2:c.12791C>A
|
XP_016864668.1:p.Thr4264Lys
|
|
XM_017009185.1:c.8975C>A
|
XP_016864674.1:p.Thr2992Lys
|
|
XM_017009186.1:c.8528C>A
|
XP_016864675.1:p.Thr2843Lys
|
|
XM_017009188.1:c.7865C>A
|
XP_016864677.1:p.Thr2622Lys
|
|
XM_024454388.1:c.12791C>A
|
XP_024310156.1:p.Thr4264Lys
|
|
XM_024454389.1:c.12380C>A
|
XP_024310157.1:p.Thr4127Lys
|
|
NM_001369.3:c.13778C>A
MANE Select
|
NP_001360.1:p.Thr4593Lys
|
|