ENST00000420175.3:c.266C>G
MANE Select
|
ENSP00000391137.2:p.Thr89Ser
|
|
ENST00000275838.5:c.266C>G
|
ENSP00000275838.1:p.Thr89Ser
|
|
ENST00000377867.7:c.272-206C>G
|
ENSP00000367098.3:n.272-206C>G
|
|
ENST00000415615.1:c.*310C>G
|
ENSP00000410871.1:n.*310C>G
|
|
ENST00000420175.2:c.266C>G
|
ENSP00000391137.2:p.Thr89Ser
|
|
NM_001142459.1:c.266C>G
|
NP_001135931.2:p.Thr89Ser
|
|
NM_001142460.1:c.266C>G
|
NP_001135932.2:p.Thr89Ser
|
|
NM_080871.3:c.272-206C>G
|
NP_543147.2:n.272-206C>G
|
|
XM_005249949.3:c.401C>G
|
XP_005250006.1:p.Thr134Ser
|
|
NM_001142459.2:c.266C>G
MANE Select
|
NP_001135931.2:p.Thr89Ser
|
|
NM_080871.4:c.272-206C>G
|
NP_543147.2:n.272-206C>G
|
|