ENST00000585482.6:c.*3425A>C
(SARM1)
MANE Select
|
ENSP00000468032.2:n.*3425A>C
|
|
ENST00000612814.5:c.1325T>G
(SLC46A1)
MANE Select
|
ENSP00000480703.1:p.Met442Arg
|
|
ENST00000582735.1:c.209T>G
(SLC46A1)
|
|
|
ENST00000585482.5:c.*3425A>C
(SARM1)
|
ENSP00000468032.2:n.*3425A>C
|
|
ENST00000612814.4:c.1325T>G
(SLC46A1)
|
ENSP00000480703.1:p.Met442Arg
|
|
ENST00000618626.1:c.1241T>G
(SLC46A1)
|
ENSP00000483652.1:p.Met414Arg
|
|
NM_001242366.2:c.1241T>G
(SLC46A1)
|
NP_001229295.1:p.Met414Arg
|
|
NM_015077.3:c.*3425A>C
(SARM1)
|
NP_055892.2:n.*3425A>C
|
|
NM_080669.5:c.1325T>G
(SLC46A1)
|
NP_542400.2:p.Met442Arg
|
|
XM_005277786.2:c.1084T>G
(SLC46A1)
|
XP_005277843.1:p.Cys362Gly
|
|
XM_005277786.3:c.1084T>G
(SLC46A1)
|
XP_005277843.1:p.Cys362Gly
|
|
XM_017024110.1:c.1103T>G
(SLC46A1)
|
XP_016879599.1:p.Met368Arg
|
|
NM_015077.4:c.*3425A>C
(SARM1)
MANE Select
|
NP_055892.2:n.*3425A>C
|
|
NM_080669.6:c.1325T>G
(SLC46A1)
MANE Select
|
NP_542400.2:p.Met442Arg
|
|
NM_001242366.3:c.1241T>G
(SLC46A1)
|
NP_001229295.1:p.Met414Arg
|
|