ENST00000355621.8:c.421A>T
MANE Select
|
ENSP00000347836.3:p.Ile141Phe
|
|
ENST00000649897.1:c.211A>T
|
ENSP00000497987.1:p.Ile71Phe
|
|
ENST00000355621.7:c.421A>T
|
ENSP00000347836.3:p.Ile141Phe
|
|
ENST00000472396.5:c.361A>T
|
ENSP00000419689.1:p.Ile121Phe
|
|
ENST00000473814.6:c.328A>T
|
ENSP00000419097.2:p.Ile110Phe
|
|
ENST00000483368.1:n.529A>T
|
|
|
ENST00000496698.5:c.322A>T
|
ENSP00000417681.1:p.Ile108Phe
|
|
NM_001202498.1:c.211A>T
|
NP_001189427.1:p.Ile71Phe
|
|
NM_003344.3:c.421A>T
|
NP_003335.1:p.Ile141Phe
|
|
NM_182697.2:c.328A>T
|
NP_874356.1:p.Ile110Phe
|
|
XM_011516547.1:c.610A>T
|
XP_011514849.1:p.Ile204Phe
|
|
NM_001202498.2:c.211A>T
|
NP_001189427.1:p.Ile71Phe
|
|
NM_003344.4:c.421A>T
MANE Select
|
NP_003335.1:p.Ile141Phe
|
|
NM_182697.3:c.328A>T
|
NP_874356.1:p.Ile110Phe
|
|