ENST00000389048.8:c.3801G=
MANE Select
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ENSP00000373700.3:p.Lys1267=
|
|
ENST00000431873.6:c.1028G=
|
|
|
ENST00000638605.1:n.678G=
|
|
|
ENST00000642122.1:c.597G=
|
ENSP00000493203.1:p.Lys199=
|
|
ENST00000389048.7:c.3801G=
|
ENSP00000373700.3:p.Lys1267=
|
|
ENST00000431873.5:c.681G=
|
ENSP00000414027.2:p.Lys227=
|
|
ENST00000618119.4:c.2670G=
|
ENSP00000482733.1:p.Lys890=
|
|
NM_004304.4:c.3801G=
|
NP_004295.2:p.Lys1267=
|
|
NM_001353765.1:c.597G=
|
NP_001340694.1:p.Lys199=
|
|
XM_024452778.1:c.954G=
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XP_024308546.1:p.Lys318=
|
|
XM_024452779.1:c.597G=
|
XP_024308547.1:p.Lys199=
|
|
NM_004304.5:c.3801G=
MANE Select
|
NP_004295.2:p.Lys1267=
|
|
NM_001353765.2:c.597G=
|
NP_001340694.1:p.Lys199=
|
|