ENST00000225964.10:c.4234G>A
MANE Select
|
ENSP00000225964.6:p.Val1412Ile
|
|
ENST00000225964.9:c.4234G>A
|
ENSP00000225964.5:p.Val1412Ile
|
|
NM_000088.3:c.4234G>A , LRG_1t1:c.4234G>A
|
NP_000079.2:p.Val1412Ile
|
|
XM_005257058.3:c.3964G>A
|
XP_005257115.2:p.Val1322Ile
|
|
XM_005257059.3:c.3316G>A
|
XP_005257116.2:p.Val1106Ile
|
|
XM_011524341.1:c.4036G>A
|
XP_011522643.1:p.Val1346Ile
|
|
XM_005257058.4:c.3964G>A
|
XP_005257115.2:p.Val1322Ile
|
|
XM_005257059.4:c.3316G>A
|
XP_005257116.2:p.Val1106Ile
|
|
NM_000088.4:c.4234G>A
MANE Select
|
NP_000079.2:p.Val1412Ile
|
|