ENST00000320185.7:c.337+16G>T
MANE Select
|
ENSP00000321797.2:n.337+16G>T
|
|
ENST00000618991.5:c.25+16G>T
|
ENSP00000484420.1:n.25+16G>T
|
|
ENST00000344255.8:c.304+16G>T
|
ENSP00000340039.3:n.304+16G>T
|
|
ENST00000320185.6:c.337+16G>T
|
ENSP00000321797.2:n.337+16G>T
|
|
ENST00000344255.7:c.304+16G>T
|
ENSP00000340039.3:n.304+16G>T
|
|
ENST00000346714.7:c.217+16G>T
|
ENSP00000344306.3:n.217+16G>T
|
|
ENST00000347978.2:c.250+16G>T
|
ENSP00000321945.2:n.250+16G>T
|
|
ENST00000469792.6:c.*301+16G>T
|
ENSP00000473299.1:n.*301+16G>T
|
|
ENST00000485728.1:n.213+16G>T
|
|
|
ENST00000618991.4:c.25+16G>T
|
ENSP00000484420.1:n.25+16G>T
|
|
NM_001206389.1:c.25+16G>T
|
NP_001193318.1:n.25+16G>T
|
|
NM_006119.4:c.250+16G>T
|
NP_006110.1:n.250+16G>T
|
|
NM_033163.3:c.337+16G>T
|
NP_149353.1:n.337+16G>T
|
|
NM_033164.3:c.304+16G>T
|
NP_149354.1:n.304+16G>T
|
|
NM_033165.3:c.217+16G>T
|
NP_149355.1:n.217+16G>T
|
|
XM_011539509.1:c.259+16G>T
|
XP_011537811.1:n.259+16G>T
|
|
NM_006119.5:c.250+16G>T
|
NP_006110.1:n.250+16G>T
|
|
NM_033163.4:c.337+16G>T
|
NP_149353.1:n.337+16G>T
|
|
NM_033164.4:c.304+16G>T
|
NP_149354.1:n.304+16G>T
|
|
NM_033165.4:c.217+16G>T
|
NP_149355.1:n.217+16G>T
|
|
NM_001206389.2:c.25+16G>T
|
NP_001193318.1:n.25+16G>T
|
|
NM_006119.6:c.250+16G>T
|
NP_006110.1:n.250+16G>T
|
|
NM_033163.5:c.337+16G>T
MANE Select
|
NP_149353.1:n.337+16G>T
|
|
NM_033165.5:c.217+16G>T
|
NP_149355.1:n.217+16G>T
|
|