ENST00000350721.9:c.7814C>T
MANE Select
|
ENSP00000343741.4:p.Thr2605Ile
|
|
ENST00000513291.2:n.6523C>T
|
|
|
ENST00000653893.1:n.2672C>T
|
|
|
ENST00000654170.1:n.2657C>T
|
|
|
ENST00000656114.1:n.2900C>T
|
|
|
ENST00000656590.1:c.6741C>T
|
|
|
ENST00000658083.1:n.2994C>T
|
|
|
ENST00000661310.1:c.7622C>T
|
ENSP00000499589.1:p.Thr2541Ile
|
|
ENST00000665483.1:n.5354C>T
|
|
|
ENST00000666447.1:n.4317C>T
|
|
|
ENST00000666943.1:n.4546C>T
|
|
|
ENST00000350721.8:c.7814C>T
|
ENSP00000343741.4:p.Thr2605Ile
|
|
ENST00000504521.5:c.403C>T
|
ENSP00000422553.1:n.403C>T
|
|
ENST00000513291.1:c.4878C>T
|
|
|
ENST00000515810.1:c.240C>T
|
ENSP00000421870.1:n.240C>T
|
|
NM_001184.3:c.7814C>T
|
NP_001175.2:p.Thr2605Ile
|
|
XM_011512924.1:c.7820C>T
|
XP_011511226.1:p.Thr2607Ile
|
|
XM_011512925.1:c.7628C>T
|
XP_011511227.1:p.Thr2543Ile
|
|
XR_924147.1:n.10571C>T
|
|
|
XR_924148.1:n.8046C>T
|
|
|
NM_001354579.1:c.7622C>T
|
NP_001341508.1:p.Thr2541Ile
|
|
XR_001740179.2:n.8040C>T
|
|
|
XR_924148.2:n.8046C>T
|
|
|
NM_001184.4:c.7814C>T
MANE Select
|
NP_001175.2:p.Thr2605Ile
|
|
NM_001354579.2:c.7622C>T
|
NP_001341508.1:p.Thr2541Ile
|
|