ENST00000389048.8:c.3497T=
MANE Select
|
ENSP00000373700.3:p.Met1166=
|
|
ENST00000431873.6:c.724T=
|
|
|
ENST00000638605.1:n.374T=
|
|
|
ENST00000642122.1:c.293T=
|
ENSP00000493203.1:p.Met98=
|
|
ENST00000389048.7:c.3497T=
|
ENSP00000373700.3:p.Met1166=
|
|
ENST00000431873.5:c.377T=
|
ENSP00000414027.2:p.Met126=
|
|
ENST00000453137.1:c.191T=
|
ENSP00000387488.1:p.Met64=
|
|
ENST00000618119.4:c.2366T=
|
ENSP00000482733.1:p.Met789=
|
|
NM_004304.4:c.3497T=
|
NP_004295.2:p.Met1166=
|
|
NM_001353765.1:c.293T=
|
NP_001340694.1:p.Met98=
|
|
XM_024452778.1:c.650T=
|
XP_024308546.1:p.Met217=
|
|
XM_024452779.1:c.293T=
|
XP_024308547.1:p.Met98=
|
|
NM_004304.5:c.3497T=
MANE Select
|
NP_004295.2:p.Met1166=
|
|
NM_001353765.2:c.293T=
|
NP_001340694.1:p.Met98=
|
|