ENST00000435881.7:c.715T>G
MANE Select
|
ENSP00000416627.1:p.Leu239Val
|
|
ENST00000246912.8:c.877T>G
|
ENSP00000246912.3:p.Leu293Val
|
|
ENST00000346833.8:c.625T>G
|
ENSP00000320913.3:p.Leu209Val
|
|
ENST00000435881.6:c.715T>G
|
ENSP00000416627.1:p.Leu239Val
|
|
ENST00000585403.5:n.922T>G
|
|
|
ENST00000588320.1:n.1191T>G
|
|
|
ENST00000590050.5:n.881T>G
|
|
|
NM_170607.2:c.877T>G
|
NP_733752.1:p.Leu293Val
|
|
NM_198204.1:c.715T>G
|
NP_937847.1:p.Leu239Val
|
|
NM_198205.1:c.625T>G
|
NP_937848.1:p.Leu209Val
|
|
NM_198204.2:c.715T>G
MANE Select
|
NP_937847.1:p.Leu239Val
|
|
NM_170607.3:c.877T>G
|
NP_733752.1:p.Leu293Val
|
|
NM_198205.2:c.625T>G
|
NP_937848.1:p.Leu209Val
|
|