ENST00000371270.6:c.1318C>T
MANE Select
|
ENSP00000360317.3:p.Leu440Phe
|
|
ENST00000371270.5:c.1318C>T
|
ENSP00000360317.3:p.Leu440Phe
|
|
ENST00000490994.6:c.*1104C>T
|
ENSP00000433314.1:n.*1104C>T
|
|
ENST00000525991.5:c.*893C>T
|
ENSP00000433842.1:n.*893C>T
|
|
ENST00000526814.5:n.1573C>T
|
|
|
ENST00000527420.5:c.*175C>T
|
ENSP00000433191.1:n.*175C>T
|
|
ENST00000527953.5:n.1612C>T
|
|
|
ENST00000531714.1:n.506C>T
|
|
|
ENST00000533320.5:n.1552C>T
|
|
|
ENST00000535898.5:c.1012C>T
|
ENSP00000445062.1:p.Leu338Phe
|
|
ENST00000539050.5:c.1108C>T
|
ENSP00000442343.2:p.Leu370Phe
|
|
ENST00000623108.3:c.1108C>T
|
ENSP00000485110.1:p.Leu370Phe
|
|
NM_000770.3:c.1318C>T
MANE Select
|
NP_000761.3:p.Leu440Phe
|
|
NM_001198853.1:c.1108C>T
|
NP_001185782.1:p.Leu370Phe
|
|
NM_001198854.1:c.1012C>T
|
NP_001185783.1:p.Leu338Phe
|
|
NM_001198855.1:c.1108C>T
|
NP_001185784.1:p.Leu370Phe
|
|
XR_945610.1:n.1453C>T
|
|
|