|
ENST00000328194.8:c.676C>G
MANE Select
|
ENSP00000328524.3:p.Leu226Val
|
|
|
ENST00000530780.2:c.*502C>G
|
ENSP00000433925.1:n.*502C>G
|
|
|
ENST00000530867.2:n.465C>G
|
|
|
|
ENST00000532696.2:n.599C>G
|
|
|
|
ENST00000679446.1:n.597C>G
|
|
|
|
ENST00000679460.1:n.465C>G
|
|
|
|
ENST00000679568.1:c.676C>G
|
ENSP00000505860.1:p.Leu226Val
|
|
|
ENST00000679745.1:n.465C>G
|
|
|
|
ENST00000679999.1:c.676C>G
|
ENSP00000505198.1:p.Leu226Val
|
|
|
ENST00000680252.1:c.465C>G
|
|
|
|
ENST00000680294.1:c.676C>G
|
ENSP00000506113.1:p.Leu226Val
|
|
|
ENST00000680470.1:c.676C>G
|
ENSP00000505975.1:p.Leu226Val
|
|
|
ENST00000680554.1:c.388C>G
|
ENSP00000505621.1:p.Leu130Val
|
|
|
ENST00000680576.1:n.465C>G
|
|
|
|
ENST00000680599.1:n.593C>G
|
|
|
|
ENST00000680742.1:c.676C>G
|
ENSP00000505206.1:p.Leu226Val
|
|
|
ENST00000680885.1:n.597C>G
|
|
|
|
ENST00000681158.1:c.465C>G
|
|
|
|
ENST00000681173.1:n.465C>G
|
|
|
|
ENST00000681203.1:c.604C>G
|
ENSP00000506456.1:p.Leu202Val
|
|
|
ENST00000681425.1:n.597C>G
|
|
|
|
ENST00000681915.1:n.465C>G
|
|
|
|
ENST00000328194.7:c.676C>G
|
ENSP00000328524.3:p.Leu226Val
|
|
|
ENST00000526707.5:c.604C>G
|
ENSP00000436780.1:p.Leu202Val
|
|
|
ENST00000530044.5:c.676C>G
|
ENSP00000435866.1:p.Leu226Val
|
|
|
ENST00000532696.1:n.431C>G
|
|
|
|
NM_001243254.1:c.676C>G
|
NP_001230183.1:p.Leu226Val
|
|
|
NM_015213.3:c.676C>G
|
NP_056028.2:p.Leu226Val
|
|
|
XM_005252832.1:c.676C>G
|
XP_005252889.1:p.Leu226Val
|
|
|
XM_011519952.1:c.676C>G
|
XP_011518254.1:p.Leu226Val
|
|
|
XR_242782.2:n.941C>G
|
|
|
|
XR_930851.1:n.941C>G
|
|
|
|
XR_930852.1:n.941C>G
|
|
|
|
XR_930853.1:n.941C>G
|
|
|
|
NM_001348749.1:c.604C>G
|
NP_001335678.1:p.Leu202Val
|
|
|
NM_001348750.1:c.388C>G
|
NP_001335679.1:p.Leu130Val
|
|
|
NR_145966.2:n.933C>G
|
|
|
|
NM_015213.4:c.676C>G
MANE Select
|
NP_056028.2:p.Leu226Val
|
|
|
NM_001243254.2:c.676C>G
|
NP_001230183.1:p.Leu226Val
|
|
|
NM_001348749.2:c.604C>G
|
NP_001335678.1:p.Leu202Val
|
|
|
NM_001348750.2:c.388C>G
|
NP_001335679.1:p.Leu130Val
|
|
