ENST00000585482.6:c.*3387A>T
(SARM1)
MANE Select
|
ENSP00000468032.2:n.*3387A>T
|
|
ENST00000612814.5:c.1363T>A
(SLC46A1)
MANE Select
|
ENSP00000480703.1:p.Phe455Ile
|
|
ENST00000582735.1:c.247T>A
(SLC46A1)
|
|
|
ENST00000585482.5:c.*3387A>T
(SARM1)
|
ENSP00000468032.2:n.*3387A>T
|
|
ENST00000612814.4:c.1363T>A
(SLC46A1)
|
ENSP00000480703.1:p.Phe455Ile
|
|
ENST00000618626.1:c.1279T>A
(SLC46A1)
|
ENSP00000483652.1:p.Phe427Ile
|
|
NM_001242366.2:c.1279T>A
(SLC46A1)
|
NP_001229295.1:p.Phe427Ile
|
|
NM_015077.3:c.*3387A>T
(SARM1)
|
NP_055892.2:n.*3387A>T
|
|
NM_080669.5:c.1363T>A
(SLC46A1)
|
NP_542400.2:p.Phe455Ile
|
|
XM_005277786.2:c.1122T>A
(SLC46A1)
|
XP_005277843.1:p.Ser374Arg
|
|
XM_005277786.3:c.1122T>A
(SLC46A1)
|
XP_005277843.1:p.Ser374Arg
|
|
XM_017024110.1:c.1141T>A
(SLC46A1)
|
XP_016879599.1:p.Phe381Ile
|
|
NM_015077.4:c.*3387A>T
(SARM1)
MANE Select
|
NP_055892.2:n.*3387A>T
|
|
NM_080669.6:c.1363T>A
(SLC46A1)
MANE Select
|
NP_542400.2:p.Phe455Ile
|
|
NM_001242366.3:c.1279T>A
(SLC46A1)
|
NP_001229295.1:p.Phe427Ile
|
|