ENST00000376199.7:c.1006T>G
|
ENSP00000365372.2:p.Phe336Val
|
|
ENST00000376207.10:c.1111T>G
MANE Select
|
ENSP00000365380.4:p.Phe371Val
|
|
ENST00000455775.7:c.1180T>G
|
ENSP00000396415.3:p.Phe394Val
|
|
ENST00000518685.6:c.1030T>G
|
ENSP00000428952.2:p.Phe344Val
|
|
ENST00000557224.6:c.1006T>G
|
ENSP00000451208.1:p.Phe336Val
|
|
ENST00000651307.1:c.*26T>G
|
ENSP00000498454.1:n.*26T>G
|
|
ENST00000376197.1:c.961T>G
|
ENSP00000365369.1:p.Phe321Val
|
|
ENST00000376199.6:c.1006T>G
|
ENSP00000365372.2:p.Phe336Val
|
|
ENST00000376207.8:c.1111T>G
|
ENSP00000365380.4:p.Phe371Val
|
|
ENST00000455775.6:c.1180T>G
|
ENSP00000396415.3:p.Phe394Val
|
|
ENST00000518685.5:c.1006T>G
|
ENSP00000428952.1:p.Phe336Val
|
|
ENST00000557224.5:c.1006T>G
|
ENSP00000451208.1:p.Phe336Val
|
|
NM_001114377.1:c.1006T>G
|
NP_001107849.1:p.Phe336Val
|
|
NM_014009.3:c.1111T>G , LRG_62t1:c.1111T>G
|
NP_054728.2:p.Phe371Val
|
|
XM_006724533.2:c.1180T>G
|
XP_006724596.2:p.Phe394Val
|
|
XM_011543915.1:c.1330T>G
|
XP_011542217.1:p.Phe444Val
|
|
XM_011543916.1:c.1330T>G
|
XP_011542218.1:p.Phe444Val
|
|
XM_011543917.1:c.1129T>G
|
XP_011542219.1:p.Phe377Val
|
|
XM_011543918.1:c.1366T>G
|
XP_011542220.1:p.Phe456Val
|
|
XM_011543919.1:c.1330T>G
|
XP_011542221.1:p.Phe444Val
|
|
XM_017029567.1:c.1057T>G
|
XP_016885056.1:p.Phe353Val
|
|
NM_001114377.2:c.1006T>G
|
NP_001107849.1:p.Phe336Val
|
|
NM_014009.4:c.1111T>G
MANE Select
|
NP_054728.2:p.Phe371Val
|
|