ENST00000367435.5:c.637T>A
MANE Select
|
ENSP00000356405.4:p.Phe213Ile
|
|
ENST00000635846.1:c.637T>A
|
ENSP00000490035.1:p.Phe213Ile
|
|
ENST00000643006.1:c.637T>A
|
ENSP00000496633.1:p.Phe213Ile
|
|
ENST00000643784.1:c.*113T>A
|
ENSP00000494944.1:n.*113T>A
|
|
ENST00000647662.1:n.538T>A
|
|
|
ENST00000648071.1:c.*613T>A
|
ENSP00000497513.1:n.*613T>A
|
|
ENST00000649606.1:n.650T>A
|
|
|
ENST00000649895.1:n.855T>A
|
|
|
ENST00000650197.1:c.637T>A
|
ENSP00000496929.1:p.Phe213Ile
|
|
ENST00000367435.3:c.637T>A
|
ENSP00000356405.3:p.Phe213Ile
|
|
NM_024529.4:c.637T>A , LRG_507t1:c.637T>A
|
NP_078805.3:p.Phe213Ile
|
|
XM_006711537.2:c.637T>A
|
XP_006711600.1:p.Phe213Ile
|
|
XM_006711537.4:c.637T>A
|
XP_006711600.1:p.Phe213Ile
|
|
NM_024529.5:c.637T>A
MANE Select
|
NP_078805.3:p.Phe213Ile
|
|