ENST00000309383.6:c.2137C>T
MANE Select
|
ENSP00000310649.1:p.Leu713Phe
|
|
ENST00000309383.5:c.2137C>T
|
ENSP00000310649.1:p.Leu713Phe
|
|
ENST00000326848.7:c.1222C>T
|
ENSP00000320853.7:p.Leu408Phe
|
|
ENST00000590333.5:c.2185C>T
|
ENSP00000468190.1:p.Leu729Phe
|
|
NM_032430.1:c.2137C>T
|
NP_115806.1:p.Leu713Phe
|
|
XM_005259327.2:c.1867C>T
|
XP_005259384.1:p.Leu623Phe
|
|
XM_011527395.1:c.1894C>T
|
XP_011525697.1:p.Leu632Phe
|
|
XR_430213.2:n.2120C>T
|
|
|
XM_005259327.3:c.1867C>T
|
XP_005259384.1:p.Leu623Phe
|
|
XM_011527395.2:c.1609C>T
|
XP_011525697.2:p.Leu537Phe
|
|
XM_024451739.1:c.1912C>T
|
XP_024307507.1:p.Leu638Phe
|
|
XR_430213.4:n.2418C>T
|
|
|
NM_032430.2:c.2137C>T
MANE Select
|
NP_115806.1:p.Leu713Phe
|
|