|
ENST00000358552.8:c.485T>G
|
ENSP00000351354.5:p.Val162Gly
|
|
|
ENST00000622520.2:c.485T>G
|
ENSP00000481181.2:p.Val162Gly
|
|
|
ENST00000693124.1:c.306T>G
|
|
|
|
ENST00000592199.6:c.488T>G
MANE Select
|
ENSP00000467512.1:p.Val163Gly
|
|
|
ENST00000676441.1:c.512T>G
|
ENSP00000502554.1:p.Val171Gly
|
|
|
ENST00000358552.7:c.497T>G
|
ENSP00000351354.4:p.Val166Gly
|
|
|
ENST00000360105.8:c.497T>G
|
ENSP00000353219.4:p.Val166Gly
|
|
|
ENST00000397661.6:c.488T>G
|
ENSP00000380781.2:p.Val163Gly
|
|
|
ENST00000585382.5:c.234+113T>G
|
ENSP00000466605.1:n.234+113T>G
|
|
|
ENST00000585575.5:c.464T>G
|
ENSP00000468794.1:p.Val155Gly
|
|
|
ENST00000586797.5:c.*319T>G
|
ENSP00000467536.1:n.*319T>G
|
|
|
ENST00000586873.1:c.347T>G
|
ENSP00000468707.1:p.Val116Gly
|
|
|
ENST00000587260.1:c.485T>G
|
ENSP00000467785.1:p.Val162Gly
|
|
|
ENST00000587760.5:c.464T>G
|
ENSP00000466389.1:p.Val155Gly
|
|
|
ENST00000588228.5:c.347T>G
|
ENSP00000466735.1:p.Val116Gly
|
|
|
ENST00000590027.1:c.347T>G
|
ENSP00000465616.1:p.Val116Gly
|
|
|
ENST00000591028.1:c.536T>G
|
ENSP00000465094.1:p.Val179Gly
|
|
|
ENST00000592199.5:c.488T>G
|
ENSP00000467512.1:p.Val163Gly
|
|
|
NM_001271043.2:c.512T>G
|
NP_001257972.1:p.Val171Gly
|
|
|
NM_001271044.2:c.464T>G
|
NP_001257973.1:p.Val155Gly
|
|
|
NM_002501.3:c.488T>G
|
NP_002492.2:p.Val163Gly
|
|
|
XM_005259917.3:c.665T>G
|
XP_005259974.1:p.Val222Gly
|
|
|
XM_005259918.3:c.488T>G
|
XP_005259975.1:p.Val163Gly
|
|
|
XM_005259919.3:c.665T>G
|
XP_005259976.1:p.Val222Gly
|
|
|
XM_005259920.3:c.464T>G
|
XP_005259977.1:p.Val155Gly
|
|
|
XM_005259921.3:c.665T>G
|
XP_005259978.1:p.Val222Gly
|
|
|
XM_005259922.3:c.665T>G
|
XP_005259979.1:p.Val222Gly
|
|
|
XM_006722760.2:c.665T>G
|
XP_006722823.1:p.Val222Gly
|
|
|
XM_011528040.1:c.536T>G
|
XP_011526342.1:p.Val179Gly
|
|
|
NM_001365902.1:c.488T>G
|
NP_001352831.1:p.Val163Gly
|
|
|
NM_001365982.1:c.488T>G
|
NP_001352911.1:p.Val163Gly
|
|
|
NM_001365983.1:c.347T>G
|
NP_001352912.1:p.Val116Gly
|
|
|
NM_001365984.1:c.485T>G
|
NP_001352913.1:p.Val162Gly
|
|
|
NM_001365985.1:c.485T>G
|
NP_001352914.1:p.Val162Gly
|
|
|
XM_005259917.4:c.665T>G
|
XP_005259974.1:p.Val222Gly
|
|
|
NM_001271044.3:c.464T>G
|
NP_001257973.1:p.Val155Gly
|
|
|
NM_001365902.2:c.488T>G
|
NP_001352831.1:p.Val163Gly
|
|
|
NM_001365982.2:c.488T>G
|
NP_001352911.1:p.Val163Gly
|
|
|
NM_001365983.2:c.347T>G
|
NP_001352912.1:p.Val116Gly
|
|
|
NM_001365984.2:c.485T>G
|
NP_001352913.1:p.Val162Gly
|
|
|
NM_001365985.2:c.485T>G
|
NP_001352914.1:p.Val162Gly
|
|
|
NM_002501.4:c.488T>G
|
NP_002492.2:p.Val163Gly
|
|
|
NM_001365902.3:c.488T>G
MANE Select
|
NP_001352831.1:p.Val163Gly
|
|
|
NM_001378404.1:c.464T>G
|
NP_001365333.1:p.Val155Gly
|
|
|
NM_001378405.1:c.536T>G
|
NP_001365334.1:p.Val179Gly
|
|
