ENST00000265104.5:c.9576G>A
MANE Select
|
ENSP00000265104.4:p.Lys3192=
|
|
ENST00000681290.1:c.9531G>A
|
ENSP00000505288.1:p.Lys3177=
|
|
ENST00000265104.4:c.9576G>A
|
ENSP00000265104.4:p.Lys3192=
|
|
ENST00000504001.3:n.288G>A
|
|
|
NM_001369.2:c.9576G>A
|
NP_001360.1:p.Lys3192=
|
|
XM_005248262.2:c.9531G>A
|
XP_005248319.1:p.Lys3177=
|
|
XM_005248262.3:c.9684G>A
|
XP_005248319.2:p.Lys3228=
|
|
XM_017009177.1:c.9684G>A
|
XP_016864666.1:p.Lys3228=
|
|
XM_017009178.1:c.8589G>A
|
XP_016864667.1:p.Lys2863=
|
|
XM_017009179.2:c.8589G>A
|
XP_016864668.1:p.Lys2863=
|
|
XM_017009180.1:c.9684G>A
|
XP_016864669.1:p.Lys3228=
|
|
XM_017009181.1:c.9684G>A
|
XP_016864670.1:p.Lys3228=
|
|
XM_017009182.1:c.9684G>A
|
XP_016864671.1:p.Lys3228=
|
|
XM_017009183.1:c.9684G>A
|
XP_016864672.1:p.Lys3228=
|
|
XM_017009185.1:c.4773G>A
|
XP_016864674.1:p.Lys1591=
|
|
XM_017009186.1:c.4326G>A
|
XP_016864675.1:p.Lys1442=
|
|
XM_017009188.1:c.3663G>A
|
XP_016864677.1:p.Lys1221=
|
|
XM_024454388.1:c.8589G>A
|
XP_024310156.1:p.Lys2863=
|
|
XM_024454389.1:c.8178G>A
|
XP_024310157.1:p.Lys2726=
|
|
NM_001369.3:c.9576G>A
MANE Select
|
NP_001360.1:p.Lys3192=
|
|