ENST00000220676.2:c.3982C>A
MANE Select
|
ENSP00000220676.1:p.Pro1328Thr
|
|
ENST00000636932.1:c.787+5576C>A
|
ENSP00000489857.1:n.787+5576C>A
|
|
ENST00000637698.1:c.787+5576C>A
|
ENSP00000490104.1:n.787+5576C>A
|
|
ENST00000220676.1:c.3982C>A
|
ENSP00000220676.1:p.Pro1328Thr
|
|
NM_006269.1:c.3982C>A
|
NP_006260.1:p.Pro1328Thr
|
|
XM_017013721.1:c.4003C>A
|
XP_016869210.1:p.Pro1335Thr
|
|
XM_017013722.1:c.3982C>A
|
XP_016869211.1:p.Pro1328Thr
|
|
NM_001375654.1:c.787+5576C>A
|
NP_001362583.1:n.787+5576C>A
|
|
NM_006269.2:c.3982C>A
MANE Select
|
NP_006260.1:p.Pro1328Thr
|
|