ENST00000225964.10:c.3152C>A
MANE Select
|
ENSP00000225964.6:p.Pro1051His
|
|
ENST00000225964.9:c.3152C>A
|
ENSP00000225964.5:p.Pro1051His
|
|
ENST00000511732.1:n.96C>A
|
|
|
NM_000088.3:c.3152C>A , LRG_1t1:c.3152C>A
|
NP_000079.2:p.Pro1051His
|
|
XM_005257058.3:c.2882C>A
|
XP_005257115.2:p.Pro961His
|
|
XM_005257059.3:c.2234C>A
|
XP_005257116.2:p.Pro745His
|
|
XM_011524341.1:c.2954C>A
|
XP_011522643.1:p.Pro985His
|
|
XM_005257058.4:c.2882C>A
|
XP_005257115.2:p.Pro961His
|
|
XM_005257059.4:c.2234C>A
|
XP_005257116.2:p.Pro745His
|
|
NM_000088.4:c.3152C>A
MANE Select
|
NP_000079.2:p.Pro1051His
|
|