ENST00000236959.14:c.1288T>A
MANE Select
|
ENSP00000236959.9:p.Ser430Thr
|
|
ENST00000236959.13:c.1288T>A
|
ENSP00000236959.9:p.Ser430Thr
|
|
ENST00000426233.1:c.293T>A
|
|
|
ENST00000435675.5:c.1285T>A
|
ENSP00000415935.1:p.Ser429Thr
|
|
ENST00000443953.5:c.*1385T>A
|
ENSP00000406792.1:n.*1385T>A
|
|
ENST00000446622.5:n.368T>A
|
|
|
ENST00000459796.1:n.99T>A
|
|
|
ENST00000467388.1:n.200T>A
|
|
|
ENST00000479093.5:n.203T>A
|
|
|
NM_004044.6:c.1288T>A
|
NP_004035.2:p.Ser430Thr
|
|
XM_017004187.2:c.1288T>A
|
XP_016859676.1:p.Ser430Thr
|
|
XM_024452919.1:c.1111T>A
|
XP_024308687.1:p.Ser371Thr
|
|
NM_004044.7:c.1288T>A
MANE Select
|
NP_004035.2:p.Ser430Thr
|
|