ENST00000265104.5:c.11759A>T
MANE Select
|
ENSP00000265104.4:p.Lys3920Ile
|
|
ENST00000681290.1:c.11714A>T
|
ENSP00000505288.1:p.Lys3905Ile
|
|
ENST00000265104.4:c.11759A>T
|
ENSP00000265104.4:p.Lys3920Ile
|
|
NM_001369.2:c.11759A>T
|
NP_001360.1:p.Lys3920Ile
|
|
XM_005248262.2:c.11714A>T
|
XP_005248319.1:p.Lys3905Ile
|
|
XM_005248262.3:c.11867A>T
|
XP_005248319.2:p.Lys3956Ile
|
|
XM_017009177.1:c.11867A>T
|
XP_016864666.1:p.Lys3956Ile
|
|
XM_017009178.1:c.10772A>T
|
XP_016864667.1:p.Lys3591Ile
|
|
XM_017009179.2:c.10772A>T
|
XP_016864668.1:p.Lys3591Ile
|
|
XM_017009180.1:c.11867A>T
|
XP_016864669.1:p.Lys3956Ile
|
|
XM_017009181.1:c.11867A>T
|
XP_016864670.1:p.Lys3956Ile
|
|
XM_017009185.1:c.6956A>T
|
XP_016864674.1:p.Lys2319Ile
|
|
XM_017009186.1:c.6509A>T
|
XP_016864675.1:p.Lys2170Ile
|
|
XM_017009188.1:c.5846A>T
|
XP_016864677.1:p.Lys1949Ile
|
|
XM_024454388.1:c.10772A>T
|
XP_024310156.1:p.Lys3591Ile
|
|
XM_024454389.1:c.10361A>T
|
XP_024310157.1:p.Lys3454Ile
|
|
NM_001369.3:c.11759A>T
MANE Select
|
NP_001360.1:p.Lys3920Ile
|
|