ENST00000478003.2:n.2187C>A
|
|
|
ENST00000682276.1:n.1804C>A
|
|
|
ENST00000682892.1:c.1906C>A
|
ENSP00000507214.1:p.Leu636Ile
|
|
ENST00000682952.1:n.1998C>A
|
|
|
ENST00000684455.1:c.1572C>A
|
|
|
ENST00000684642.1:c.1756C>A
|
ENSP00000507355.1:p.Leu586Ile
|
|
ENST00000684740.1:n.2537C>A
|
|
|
ENST00000303236.9:c.2359C>A
MANE Select
|
ENSP00000307235.3:p.Leu787Ile
|
|
ENST00000652099.1:c.2553C>A
|
|
|
ENST00000652736.1:n.2235C>A
|
|
|
ENST00000303236.7:c.2359C>A
|
ENSP00000307235.3:p.Leu787Ile
|
|
ENST00000415570.1:c.1996C>A
|
ENSP00000412076.1:p.Leu666Ile
|
|
ENST00000419748.5:c.1906C>A
|
ENSP00000408325.1:p.Leu636Ile
|
|
ENST00000470706.1:n.49-47C>A
|
|
|
NM_001313915.1:c.1906C>A
|
NP_001300844.1:p.Leu636Ile
|
|
NM_004836.5:c.2359C>A
|
NP_004827.4:p.Leu787Ile
|
|
NM_004836.6:c.2359C>A
|
NP_004827.4:p.Leu787Ile
|
|
NR_110236.1:n.1261G>T
|
|
|
XM_005264649.3:c.1675C>A
|
XP_005264706.1:p.Leu559Ile
|
|
XM_017005376.2:c.1675C>A
|
XP_016860865.1:p.Leu559Ile
|
|
NM_004836.7:c.2359C>A
MANE Select
|
NP_004827.4:p.Leu787Ile
|
|
NM_001313915.2:c.1906C>A
|
NP_001300844.1:p.Leu636Ile
|
|