ENST00000225964.10:c.4216T>A
MANE Select
|
ENSP00000225964.6:p.Phe1406Ile
|
|
ENST00000225964.9:c.4216T>A
|
ENSP00000225964.5:p.Phe1406Ile
|
|
NM_000088.3:c.4216T>A , LRG_1t1:c.4216T>A
|
NP_000079.2:p.Phe1406Ile
|
|
XM_005257058.3:c.3946T>A
|
XP_005257115.2:p.Phe1316Ile
|
|
XM_005257059.3:c.3298T>A
|
XP_005257116.2:p.Phe1100Ile
|
|
XM_011524341.1:c.4018T>A
|
XP_011522643.1:p.Phe1340Ile
|
|
XM_005257058.4:c.3946T>A
|
XP_005257115.2:p.Phe1316Ile
|
|
XM_005257059.4:c.3298T>A
|
XP_005257116.2:p.Phe1100Ile
|
|
NM_000088.4:c.4216T>A
MANE Select
|
NP_000079.2:p.Phe1406Ile
|
|