ENST00000297784.10:c.2003+197G>T
MANE Select
|
ENSP00000297784.6:n.2003+197G>T
|
|
ENST00000644967.1:c.*443+197G>T
|
ENSP00000496159.1:n.*443+197G>T
|
|
ENST00000645053.1:c.1258-5591G>T
|
ENSP00000493838.1:n.1258-5591G>T
|
|
ENST00000645208.2:c.2003+197G>T
|
ENSP00000494684.1:n.2003+197G>T
|
|
ENST00000645773.1:c.1877+197G>T
|
ENSP00000493698.1:n.1877+197G>T
|
|
ENST00000645787.1:n.2146+197G>T
|
|
|
ENST00000646619.1:c.1565+197G>T
|
ENSP00000493726.1:n.1565+197G>T
|
|
ENST00000651183.1:c.1565+197G>T
|
ENSP00000498723.1:n.1565+197G>T
|
|
ENST00000297784.9:c.2003+197G>T
|
ENSP00000297784.5:n.2003+197G>T
|
|
ENST00000340019.4:c.2003+197G>T
|
ENSP00000341433.3:n.2003+197G>T
|
|
ENST00000469455.1:n.484+197G>T
|
|
|
ENST00000486417.5:n.901+197G>T
|
|
|
NM_138691.2:c.2003+197G>T
|
NP_619636.2:n.2003+197G>T
|
|
XM_011518213.1:c.2591+197G>T
|
XP_011516515.1:n.2591+197G>T
|
|
XM_017014256.1:c.2006+197G>T
|
XP_016869745.1:n.2006+197G>T
|
|
NM_138691.3:c.2003+197G>T
MANE Select
|
NP_619636.2:n.2003+197G>T
|
|