|
NM_145045.5:c.244+1G>T
MANE Select
|
NP_659482.3:n.244+1G>T
|
|
ENST00000356392.9:c.244+1G>T
MANE Select
|
ENSP00000348757.3:n.244+1G>T
|
|
NM_001302453.1:c.82+918G>T
|
NP_001289382.1:n.82+918G>T
|
|
NM_001302454.1:c.244+1G>T
|
NP_001289383.1:n.244+1G>T
|
|
NM_001302454.2:c.244+1G>T
|
NP_001289383.1:n.244+1G>T
|
|
NM_145045.4:c.244+1G>T
|
NP_659482.3:n.244+1G>T
|
|
ENST00000356392.8:c.244+1G>T
|
ENSP00000348757.3:n.244+1G>T
|
|
ENST00000586836.5:c.-330+918G>T
|
ENSP00000467429.1:n.-330+918G>T
|
|
ENST00000591179.5:c.244+1G>T
|
ENSP00000466800.1:n.244+1G>T
|
|
ENST00000591345.5:c.244+1G>T
|
ENSP00000467313.1:n.244+1G>T
|
|
ENST00000593281.1:n.127+1G>T
|
|
|
XM_017026241.1:c.244+1G>T
|
XP_016881730.1:n.244+1G>T
|