ENST00000683611.1:n.1168G>A
|
|
|
ENST00000265104.5:c.13835G>A
MANE Select
|
ENSP00000265104.4:p.Trp4612Ter
|
|
ENST00000681290.1:c.13790G>A
|
ENSP00000505288.1:p.Trp4597Ter
|
|
ENST00000265104.4:c.13835G>A
|
ENSP00000265104.4:p.Trp4612Ter
|
|
NM_001369.2:c.13835G>A
|
NP_001360.1:p.Trp4612Ter
|
|
XM_005248262.2:c.13790G>A
|
XP_005248319.1:p.Trp4597Ter
|
|
XM_005248262.3:c.13943G>A
|
XP_005248319.2:p.Trp4648Ter
|
|
XM_017009177.1:c.13523G>A
|
XP_016864666.1:p.Trp4508Ter
|
|
XM_017009178.1:c.12848G>A
|
XP_016864667.1:p.Trp4283Ter
|
|
XM_017009179.2:c.12848G>A
|
XP_016864668.1:p.Trp4283Ter
|
|
XM_017009185.1:c.9032G>A
|
XP_016864674.1:p.Trp3011Ter
|
|
XM_017009186.1:c.8585G>A
|
XP_016864675.1:p.Trp2862Ter
|
|
XM_017009188.1:c.7922G>A
|
XP_016864677.1:p.Trp2641Ter
|
|
XM_024454388.1:c.12848G>A
|
XP_024310156.1:p.Trp4283Ter
|
|
XM_024454389.1:c.12437G>A
|
XP_024310157.1:p.Trp4146Ter
|
|
NM_001369.3:c.13835G>A
MANE Select
|
NP_001360.1:p.Trp4612Ter
|
|