ENST00000220676.2:c.3741T>C
MANE Select
|
ENSP00000220676.1:p.Pro1247=
|
|
ENST00000636932.1:c.787+5335T>C
|
ENSP00000489857.1:n.787+5335T>C
|
|
ENST00000637698.1:c.787+5335T>C
|
ENSP00000490104.1:n.787+5335T>C
|
|
ENST00000220676.1:c.3741T>C
|
ENSP00000220676.1:p.Pro1247=
|
|
NM_006269.1:c.3741T>C
|
NP_006260.1:p.Pro1247=
|
|
XM_017013721.1:c.3762T>C
|
XP_016869210.1:p.Pro1254=
|
|
XM_017013722.1:c.3741T>C
|
XP_016869211.1:p.Pro1247=
|
|
NM_001375654.1:c.787+5335T>C
|
NP_001362583.1:n.787+5335T>C
|
|
NM_006269.2:c.3741T>C
MANE Select
|
NP_006260.1:p.Pro1247=
|
|