ENST00000683611.1:n.1172G>A
|
|
|
ENST00000265104.5:c.13839G>A
MANE Select
|
ENSP00000265104.4:p.Val4613=
|
|
ENST00000681290.1:c.13794G>A
|
ENSP00000505288.1:p.Val4598=
|
|
ENST00000265104.4:c.13839G>A
|
ENSP00000265104.4:p.Val4613=
|
|
NM_001369.2:c.13839G>A
|
NP_001360.1:p.Val4613=
|
|
XM_005248262.2:c.13794G>A
|
XP_005248319.1:p.Val4598=
|
|
XM_005248262.3:c.13947G>A
|
XP_005248319.2:p.Val4649=
|
|
XM_017009177.1:c.13527G>A
|
XP_016864666.1:p.Val4509=
|
|
XM_017009178.1:c.12852G>A
|
XP_016864667.1:p.Val4284=
|
|
XM_017009179.2:c.12852G>A
|
XP_016864668.1:p.Val4284=
|
|
XM_017009185.1:c.9036G>A
|
XP_016864674.1:p.Val3012=
|
|
XM_017009186.1:c.8589G>A
|
XP_016864675.1:p.Val2863=
|
|
XM_017009188.1:c.7926G>A
|
XP_016864677.1:p.Val2642=
|
|
XM_024454388.1:c.12852G>A
|
XP_024310156.1:p.Val4284=
|
|
XM_024454389.1:c.12441G>A
|
XP_024310157.1:p.Val4147=
|
|
NM_001369.3:c.13839G>A
MANE Select
|
NP_001360.1:p.Val4613=
|
|