ENST00000220420.10:c.814C>A
MANE Select
|
ENSP00000220420.5:p.Pro272Thr
|
|
ENST00000635871.1:n.283C>A
|
|
|
ENST00000220420.9:c.814C>A
|
ENSP00000220420.5:p.Pro272Thr
|
|
ENST00000349114.8:c.568C>A
|
ENSP00000220419.8:p.Pro190Thr
|
|
ENST00000610827.4:c.811C>A
|
ENSP00000479732.1:p.Pro271Thr
|
|
ENST00000611276.4:c.565C>A
|
ENSP00000482542.1:p.Pro189Thr
|
|
ENST00000622115.1:c.817C>A
|
ENSP00000479638.1:p.Pro273Thr
|
|
NM_004245.3:c.568C>A
|
NP_004236.1:p.Pro190Thr
|
|
NM_201631.3:c.814C>A
|
NP_963925.2:p.Pro272Thr
|
|
XM_011522229.1:c.814C>A
|
XP_011520531.1:p.Pro272Thr
|
|
XR_931948.1:n.988C>A
|
|
|
NM_004245.4:c.568C>A
|
NP_004236.1:p.Pro190Thr
|
|
NM_201631.4:c.814C>A
MANE Select
|
NP_963925.2:p.Pro272Thr
|
|