ENST00000297784.10:c.1999T>G
MANE Select
|
ENSP00000297784.6:p.Phe667Val
|
|
ENST00000644967.1:c.*439T>G
|
ENSP00000496159.1:n.*439T>G
|
|
ENST00000645053.1:c.1258-5792T>G
|
ENSP00000493838.1:n.1258-5792T>G
|
|
ENST00000645208.2:c.1999T>G
|
ENSP00000494684.1:p.Phe667Val
|
|
ENST00000645773.1:c.1873T>G
|
ENSP00000493698.1:p.Phe625Val
|
|
ENST00000645787.1:n.2142T>G
|
|
|
ENST00000646619.1:c.1561T>G
|
ENSP00000493726.1:p.Phe521Val
|
|
ENST00000651183.1:c.1561T>G
|
ENSP00000498723.1:p.Phe521Val
|
|
ENST00000297784.9:c.1999T>G
|
ENSP00000297784.5:p.Phe667Val
|
|
ENST00000340019.4:c.1999T>G
|
ENSP00000341433.3:p.Phe667Val
|
|
ENST00000469455.1:n.480T>G
|
|
|
ENST00000486417.5:n.897T>G
|
|
|
NM_138691.2:c.1999T>G
|
NP_619636.2:p.Phe667Val
|
|
XM_011518213.1:c.2587T>G
|
XP_011516515.1:p.Phe863Val
|
|
XM_017014256.1:c.2002T>G
|
XP_016869745.1:p.Phe668Val
|
|
NM_138691.3:c.1999T>G
MANE Select
|
NP_619636.2:p.Phe667Val
|
|