ENST00000224721.12:c.6398A>T
MANE Select
|
ENSP00000224721.9:p.Asp2133Val
|
|
ENST00000224721.10:c.6413A>T
|
ENSP00000224721.8:p.Asp2138Val
|
|
ENST00000622827.4:c.6398A>T
|
ENSP00000483211.1:p.Asp2133Val
|
|
NM_022124.5:c.6398A>T
|
NP_071407.4:p.Asp2133Val
|
|
XM_006717940.2:c.6593A>T
|
XP_006718003.1:p.Asp2198Val
|
|
XM_006717942.2:c.6527A>T
|
XP_006718005.1:p.Asp2176Val
|
|
XM_011540039.1:c.6590A>T
|
XP_011538341.1:p.Asp2197Val
|
|
XM_011540040.1:c.6587A>T
|
XP_011538342.1:p.Asp2196Val
|
|
XM_011540041.1:c.6533A>T
|
XP_011538343.1:p.Asp2178Val
|
|
XM_011540042.1:c.6577+16A>T
|
XP_011538344.1:n.6577+16A>T
|
|
XM_011540043.1:c.6593A>T
|
XP_011538345.1:p.Asp2198Val
|
|
XM_011540044.1:c.6458A>T
|
XP_011538346.1:p.Asp2153Val
|
|
XM_011540045.1:c.6593A>T
|
XP_011538347.1:p.Asp2198Val
|
|
XM_011540046.1:c.6053A>T
|
XP_011538348.1:p.Asp2018Val
|
|
XM_011540047.1:c.5411A>T
|
XP_011538349.1:p.Asp1804Val
|
|
XM_011540048.1:c.6593A>T
|
XP_011538350.1:p.Asp2198Val
|
|
XM_011540049.1:c.6593A>T
|
XP_011538351.1:p.Asp2198Val
|
|
XM_011540050.1:c.6593A>T
|
XP_011538352.1:p.Asp2198Val
|
|
XM_011540051.1:c.6593A>T
|
XP_011538353.1:p.Asp2198Val
|
|
XM_011540052.1:c.2921A>T
|
XP_011538354.1:p.Asp974Val
|
|
XR_945796.1:n.6836A>T
|
|
|
NM_022124.6:c.6398A>T
MANE Select
|
NP_071407.4:p.Asp2133Val
|
|