|
NM_001010867.4:c.979A>T
MANE Select
|
NP_001010867.1:p.Ile327Phe
|
|
ENST00000366711.4:c.979A>T
MANE Select
|
ENSP00000355672.3:p.Ile327Phe
|
|
NM_001010867.2:c.979A>T
|
NP_001010867.1:p.Ile327Phe
|
|
NM_001010867.3:c.979A>T
|
NP_001010867.1:p.Ile327Phe
|
|
NM_001310327.1:c.400A>T
|
NP_001297256.1:p.Ile134Phe
|
|
NM_001310327.2:c.400A>T
|
NP_001297256.1:p.Ile134Phe
|
|
ENST00000366711.3:c.979A>T
|
ENSP00000355672.3:p.Ile327Phe
|
|
ENST00000484749.5:n.2979A>T
|
|
|
ENST00000546123.2:n.699A>T
|
|
|
XM_006711753.2:c.679+392A>T
|
XP_006711816.1:n.679+392A>T
|