ENST00000264228.9:c.309T>G
MANE Select
|
ENSP00000264228.4:p.Pro103=
|
|
ENST00000677177.2:c.22T>G
|
|
|
ENST00000678717.1:n.206T>G
|
|
|
ENST00000679351.1:c.309T>G
|
ENSP00000505676.1:p.Pro103=
|
|
ENST00000679707.1:c.309T>G
|
ENSP00000505713.1:p.Pro103=
|
|
ENST00000679836.1:c.309T>G
|
ENSP00000506601.1:p.Pro103=
|
|
ENST00000680700.1:c.309T>G
|
ENSP00000504926.1:p.Pro103=
|
|
ENST00000264228.8:c.309T>G
|
ENSP00000264228.4:p.Pro103=
|
|
ENST00000505210.1:c.234T>G
|
ENSP00000424714.1:p.Pro78=
|
|
ENST00000514398.1:n.318T>G
|
|
|
NM_024592.4:c.309T>G
|
NP_078868.1:p.Pro103=
|
|
XM_005265766.2:c.309T>G
|
XP_005265823.1:p.Pro103=
|
|
XM_005265767.2:c.309T>G
|
XP_005265824.1:p.Pro103=
|
|
XM_005265766.4:c.309T>G
|
XP_005265823.1:p.Pro103=
|
|
XM_005265767.3:c.309T>G
|
XP_005265824.1:p.Pro103=
|
|
XM_017008601.1:c.174T>G
|
XP_016864090.1:p.Pro58=
|
|
NM_024592.5:c.309T>G
MANE Select
|
NP_078868.1:p.Pro103=
|
|