ENST00000420175.3:c.162T>A
MANE Select
|
ENSP00000391137.2:p.Pro54=
|
|
ENST00000275838.5:c.162T>A
|
ENSP00000275838.1:p.Pro54=
|
|
ENST00000377867.7:c.272-310T>A
|
ENSP00000367098.3:n.272-310T>A
|
|
ENST00000415615.1:c.*206T>A
|
ENSP00000410871.1:n.*206T>A
|
|
ENST00000420175.2:c.162T>A
|
ENSP00000391137.2:p.Pro54=
|
|
NM_001142459.1:c.162T>A
|
NP_001135931.2:p.Pro54=
|
|
NM_001142460.1:c.162T>A
|
NP_001135932.2:p.Pro54=
|
|
NM_080871.3:c.272-310T>A
|
NP_543147.2:n.272-310T>A
|
|
XM_005249949.3:c.297T>A
|
XP_005250006.1:p.Pro99=
|
|
NM_001142459.2:c.162T>A
MANE Select
|
NP_001135931.2:p.Pro54=
|
|
NM_080871.4:c.272-310T>A
|
NP_543147.2:n.272-310T>A
|
|