ENST00000340850.10:c.2839G>T
|
ENSP00000344570.5:p.Gly947Trp
|
|
ENST00000377728.8:c.2839G>T
MANE Select
|
ENSP00000366957.3:p.Gly947Trp
|
|
ENST00000377740.5:c.2839G>T
|
ENSP00000366969.4:p.Gly947Trp
|
|
ENST00000377748.6:c.3013G>T
|
ENSP00000366977.2:p.Gly1005Trp
|
|
ENST00000400913.6:c.2839G>T
|
ENSP00000383704.1:p.Gly947Trp
|
|
ENST00000400915.8:c.2950G>T
|
ENSP00000383706.4:p.Gly984Trp
|
|
ENST00000489097.6:n.3315G>T
|
|
|
ENST00000535355.6:c.3046G>T
|
ENSP00000441445.1:p.Gly1016Trp
|
|
ENST00000537245.6:c.2950G>T
|
ENSP00000439625.2:p.Gly984Trp
|
|
ENST00000673471.2:c.3136G>T
|
ENSP00000500749.1:p.Gly1046Trp
|
|
ENST00000674790.1:c.*3051G>T
|
ENSP00000502815.1:n.*3051G>T
|
|
ENST00000675123.1:c.2250-104G>T
|
ENSP00000502132.1:n.2250-104G>T
|
|
ENST00000675548.1:c.*2667G>T
|
ENSP00000502684.1:n.*2667G>T
|
|
ENST00000675694.1:c.2839G>T
|
ENSP00000501925.1:p.Gly947Trp
|
|
ENST00000675976.1:c.712G>T
|
ENSP00000501611.1:p.Gly238Trp
|
|
ENST00000340850.9:c.2839G>T
|
ENSP00000344570.5:p.Gly947Trp
|
|
ENST00000377725.5:c.2738-99G>T
|
ENSP00000366954.1:n.2738-99G>T
|
|
ENST00000377728.7:c.2839G>T
|
ENSP00000366957.3:p.Gly947Trp
|
|
ENST00000377732.5:c.2950G>T
|
ENSP00000366961.1:p.Gly984Trp
|
|
ENST00000377740.4:c.2481-104G>T
|
ENSP00000366969.3:n.2481-104G>T
|
|
ENST00000377748.5:c.3070G>T
|
ENSP00000366977.1:p.Gly1024Trp
|
|
ENST00000400913.5:c.2839G>T
|
ENSP00000383704.1:p.Gly947Trp
|
|
ENST00000400915.7:c.3007G>T
|
ENSP00000383706.3:p.Gly1003Trp
|
|
ENST00000487949.4:n.2041G>T
|
|
|
ENST00000489097.5:n.3315G>T
|
|
|
ENST00000535355.5:c.3046G>T
|
ENSP00000441445.1:p.Gly1016Trp
|
|
ENST00000537245.5:c.3076G>T
|
ENSP00000439625.1:p.Gly1026Trp
|
|
NM_001042663.1:c.3007G>T
|
NP_001036128.1:p.Gly1003Trp
|
|
NM_001042664.1:c.2839G>T
|
NP_001036129.1:p.Gly947Trp
|
|
NM_001042665.1:c.2839G>T
|
NP_001036130.1:p.Gly947Trp
|
|
NM_001265592.1:c.3076G>T
|
NP_001252521.1:p.Gly1026Trp
|
|
NM_001265593.1:c.3046G>T
|
NP_001252522.1:p.Gly1016Trp
|
|
NM_001265594.1:c.2738-99G>T
|
NP_001252523.1:n.2738-99G>T
|
|
NM_020631.4:c.2839G>T
|
NP_065682.2:p.Gly947Trp
|
|
NM_198681.3:c.3070G>T
|
NP_941374.2:p.Gly1024Trp
|
|
NM_001042663.2:c.3007G>T
|
NP_001036128.1:p.Gly1003Trp
|
|
NM_001265594.2:c.2738-99G>T
|
NP_001252523.1:n.2738-99G>T
|
|
NM_020631.5:c.2839G>T
|
NP_065682.2:p.Gly947Trp
|
|
NM_001042663.3:c.2950G>T
|
NP_001036128.2:p.Gly984Trp
|
|
NM_001265592.2:c.2950G>T
|
NP_001252521.2:p.Gly984Trp
|
|
NM_020631.6:c.2839G>T
MANE Select
|
NP_065682.2:p.Gly947Trp
|
|
NM_198681.4:c.2839G>T
|
NP_941374.3:p.Gly947Trp
|
|