ENST00000299314.12:c.2842T>G
MANE Select
|
ENSP00000299314.7:p.Phe948Val
|
|
ENST00000299314.11:c.2842T>G
|
ENSP00000299314.7:p.Phe948Val
|
|
NM_024312.4:c.2842T>G
|
NP_077288.2:p.Phe948Val
|
|
XM_006719593.2:c.2842T>G
|
XP_006719656.1:p.Phe948Val
|
|
XM_011538731.1:c.2761T>G
|
XP_011537033.1:p.Phe921Val
|
|
XM_006719593.3:c.2842T>G
|
XP_006719656.1:p.Phe948Val
|
|
XM_011538731.2:c.2761T>G
|
XP_011537033.1:p.Phe921Val
|
|
XM_017019961.1:c.2626T>G
|
XP_016875450.1:p.Phe876Val
|
|
XM_017019962.2:c.1615T>G
|
XP_016875451.1:p.Phe539Val
|
|
NM_024312.5:c.2842T>G
MANE Select
|
NP_077288.2:p.Phe948Val
|
|