ENST00000481478.2:c.6426C>A
|
ENSP00000418014.2:p.Leu2142=
|
|
ENST00000636581.2:n.1755C>A
|
|
|
ENST00000636633.2:n.3365C>A
|
|
|
ENST00000636999.2:n.1801C>A
|
|
|
ENST00000288139.11:c.6426C>A
MANE Plus Clinical
|
ENSP00000288139.3:p.Leu2142=
|
|
ENST00000350061.11:c.6366C>A
MANE Select
|
ENSP00000288133.5:p.Leu2122=
|
|
ENST00000422281.7:c.6294C>A
|
ENSP00000409174.2:p.Leu2098=
|
|
ENST00000636448.1:c.2487C>A
|
|
|
ENST00000636570.1:c.6321C>A
|
ENSP00000490183.1:p.Leu2107=
|
|
ENST00000636581.1:n.1755C>A
|
|
|
ENST00000636629.1:n.1738C>A
|
|
|
ENST00000636633.1:n.3365C>A
|
|
|
ENST00000636999.1:n.1793C>A
|
|
|
ENST00000637424.1:c.6393C>A
|
ENSP00000489769.1:p.Leu2131=
|
|
ENST00000288139.8:c.6426C>A
|
ENSP00000288139.3:p.Leu2142=
|
|
ENST00000350061.9:c.6366C>A
|
ENSP00000288133.5:p.Leu2122=
|
|
ENST00000422281.6:c.6294C>A
|
ENSP00000409174.2:p.Leu2098=
|
|
ENST00000481478.1:c.5445C>A
|
ENSP00000418014.1:p.Leu1815=
|
|
NM_000720.3:c.6426C>A
|
NP_000711.1:p.Leu2142=
|
|
NM_001128839.2:c.6294C>A
|
NP_001122311.1:p.Leu2098=
|
|
NM_001128840.2:c.6366C>A
|
NP_001122312.1:p.Leu2122=
|
|
XM_005265448.2:c.6321C>A
|
XP_005265505.1:p.Leu2107=
|
|
XM_011534094.1:c.6621C>A
|
XP_011532396.1:p.Leu2207=
|
|
XM_011534095.1:c.6510C>A
|
XP_011532397.1:p.Leu2170=
|
|
XM_011534096.1:c.6432C>A
|
XP_011532398.1:p.Leu2144=
|
|
XM_011534097.1:c.6084C>A
|
XP_011532399.1:p.Leu2028=
|
|
XM_011534098.1:c.6084C>A
|
XP_011532400.1:p.Leu2028=
|
|
XM_011534099.1:c.5709C>A
|
XP_011532401.1:p.Leu1903=
|
|
XM_011534100.1:c.6516C>A
|
XP_011532402.1:p.Leu2172=
|
|
XM_005265448.3:c.6321C>A
|
XP_005265505.1:p.Leu2107=
|
|
XM_011534094.2:c.6621C>A
|
XP_011532396.1:p.Leu2207=
|
|
XM_011534096.2:c.6432C>A
|
XP_011532398.1:p.Leu2144=
|
|
XM_011534097.2:c.6084C>A
|
XP_011532399.1:p.Leu2028=
|
|
XM_011534099.2:c.5709C>A
|
XP_011532401.1:p.Leu1903=
|
|
XM_011534100.2:c.6516C>A
|
XP_011532402.1:p.Leu2172=
|
|
XM_017007137.1:c.6621C>A
|
XP_016862626.1:p.Leu2207=
|
|
XM_017007138.1:c.6618C>A
|
XP_016862627.1:p.Leu2206=
|
|
XM_017007139.1:c.6594C>A
|
XP_016862628.1:p.Leu2198=
|
|
XM_017007140.1:c.6561C>A
|
XP_016862629.1:p.Leu2187=
|
|
XM_017007141.1:c.6561C>A
|
XP_016862630.1:p.Leu2187=
|
|
XM_017007142.1:c.6537C>A
|
XP_016862631.1:p.Leu2179=
|
|
XM_017007143.1:c.6537C>A
|
XP_016862632.1:p.Leu2179=
|
|
XM_017007144.1:c.6537C>A
|
XP_016862633.1:p.Leu2179=
|
|
XM_017007145.1:c.6492C>A
|
XP_016862634.1:p.Leu2164=
|
|
NM_001128840.3:c.6366C>A
MANE Select
|
NP_001122312.1:p.Leu2122=
|
|
NM_000720.4:c.6426C>A
MANE Plus Clinical
|
NP_000711.1:p.Leu2142=
|
|
NM_001128839.3:c.6294C>A
|
NP_001122311.1:p.Leu2098=
|
|