ENST00000645828.1:n.2804T>G
|
|
|
ENST00000651671.1:c.4997T>G
MANE Select
|
ENSP00000498587.1:p.Leu1666Arg
|
|
ENST00000679595.1:c.4997T>G
|
ENSP00000506241.1:p.Leu1666Arg
|
|
ENST00000680133.1:c.4883T>G
|
ENSP00000505319.1:p.Leu1628Arg
|
|
ENST00000680218.1:c.4877T>G
|
ENSP00000505339.1:p.Leu1626Arg
|
|
ENST00000680668.1:c.4883T>G
|
ENSP00000506336.1:p.Leu1628Arg
|
|
ENST00000680778.1:c.2594T>G
|
ENSP00000506033.1:p.Leu865Arg
|
|
ENST00000680924.1:c.*2397T>G
|
ENSP00000506031.1:n.*2397T>G
|
|
ENST00000681135.1:c.*2606T>G
|
ENSP00000506636.1:n.*2606T>G
|
|
ENST00000681298.1:n.1810T>G
|
|
|
ENST00000681454.1:c.*4233T>G
|
ENSP00000505763.1:n.*4233T>G
|
|
ENST00000277541.6:c.4997T>G
|
ENSP00000277541.6:p.Leu1666Arg
|
|
ENST00000494783.1:n.152T>G
|
|
|
NM_017617.3:c.4997T>G
|
NP_060087.3:p.Leu1666Arg
|
|
XM_011518717.1:c.4298T>G
|
XP_011517019.1:p.Leu1433Arg
|
|
NM_017617.5:c.4997T>G
MANE Select
|
NP_060087.3:p.Leu1666Arg
|
|
XM_011518717.2:c.4274T>G
|
XP_011517019.2:p.Leu1425Arg
|
|