|
ENST00000682424.1:c.337G>T
|
ENSP00000507321.1:p.Val113Leu
|
|
|
ENST00000299427.12:c.451G>T
MANE Select
|
ENSP00000299427.6:p.Val151Leu
|
|
|
ENST00000428886.7:n.539G>T
|
|
|
|
ENST00000436873.7:c.255G>T
|
|
|
|
ENST00000524788.2:n.1463G>T
|
|
|
|
ENST00000524903.2:n.1579G>T
|
|
|
|
ENST00000528571.6:c.*191G>T
|
ENSP00000434647.1:n.*191G>T
|
|
|
ENST00000528807.2:n.107G>T
|
|
|
|
ENST00000530040.2:n.479+1G>T
|
|
|
|
ENST00000533371.6:c.-279G>T
|
ENSP00000437066.1:n.-279G>T
|
|
|
ENST00000534644.6:n.452G>T
|
|
|
|
ENST00000642892.1:c.-226G>T
|
ENSP00000494165.1:n.-226G>T
|
|
|
ENST00000643439.1:c.*191G>T
|
ENSP00000495849.1:n.*191G>T
|
|
|
ENST00000643479.1:n.480G>T
|
|
|
|
ENST00000643516.1:c.338G>T
|
|
|
|
ENST00000644151.1:n.1743G>T
|
|
|
|
ENST00000644218.1:c.451G>T
|
ENSP00000493574.1:p.Val151Leu
|
|
|
ENST00000644683.1:c.450+1G>T
|
ENSP00000494085.1:n.450+1G>T
|
|
|
ENST00000644810.1:c.230-205G>T
|
ENSP00000495895.1:n.230-205G>T
|
|
|
ENST00000644831.1:n.480G>T
|
|
|
|
ENST00000644933.1:c.-279G>T
|
ENSP00000496133.1:n.-279G>T
|
|
|
ENST00000645020.1:n.1479G>T
|
|
|
|
ENST00000645285.1:c.-279G>T
|
ENSP00000495058.1:n.-279G>T
|
|
|
ENST00000645331.1:n.670G>T
|
|
|
|
ENST00000645620.1:c.-222+1G>T
|
ENSP00000493657.1:n.-222+1G>T
|
|
|
ENST00000646777.1:n.480G>T
|
|
|
|
ENST00000647016.1:n.784G>T
|
|
|
|
ENST00000647152.1:c.-279G>T
|
ENSP00000495893.1:n.-279G>T
|
|
|
ENST00000647209.1:c.*320G>T
|
ENSP00000495558.1:n.*320G>T
|
|
|
ENST00000647346.1:n.1471G>T
|
|
|
|
ENST00000299427.10:c.451G>T
|
ENSP00000299427.6:p.Val151Leu
|
|
|
ENST00000428886.6:n.473G>T
|
|
|
|
ENST00000436873.6:c.450+1G>T
|
ENSP00000398136.2:n.450+1G>T
|
|
|
ENST00000524788.1:n.4G>T
|
|
|
|
ENST00000528571.5:c.*191G>T
|
ENSP00000434647.1:n.*191G>T
|
|
|
ENST00000533371.5:c.-279G>T
|
ENSP00000437066.1:n.-279G>T
|
|
|
ENST00000534644.5:n.436G>T
|
|
|
|
ENST00000611494.4:c.451G>T
|
ENSP00000484546.1:p.Val151Leu
|
|
|
NM_000391.3:c.451G>T
|
NP_000382.3:p.Val151Leu
|
|
|
NM_000391.4:c.451G>T
MANE Select
|
NP_000382.3:p.Val151Leu
|
|
