ENST00000389048.8:c.3529C>T
MANE Select
|
ENSP00000373700.3:p.Gln1177Ter
|
|
ENST00000431873.6:c.756C>T
|
|
|
ENST00000638605.1:n.406C>T
|
|
|
ENST00000642122.1:c.325C>T
|
ENSP00000493203.1:p.Gln109Ter
|
|
ENST00000389048.7:c.3529C>T
|
ENSP00000373700.3:p.Gln1177Ter
|
|
ENST00000431873.5:c.409C>T
|
ENSP00000414027.2:p.Gln137Ter
|
|
ENST00000618119.4:c.2398C>T
|
ENSP00000482733.1:p.Gln800Ter
|
|
NM_004304.4:c.3529C>T
|
NP_004295.2:p.Gln1177Ter
|
|
NM_001353765.1:c.325C>T
|
NP_001340694.1:p.Gln109Ter
|
|
XM_024452778.1:c.682C>T
|
XP_024308546.1:p.Gln228Ter
|
|
XM_024452779.1:c.325C>T
|
XP_024308547.1:p.Gln109Ter
|
|
NM_004304.5:c.3529C>T
MANE Select
|
NP_004295.2:p.Gln1177Ter
|
|
NM_001353765.2:c.325C>T
|
NP_001340694.1:p.Gln109Ter
|
|