|
ENST00000358671.10:c.646+248G>T
MANE Select
|
ENSP00000351497.5:n.646+248G>T
|
|
|
ENST00000236937.13:c.646+248G>T
|
ENSP00000236937.9:n.646+248G>T
|
|
|
ENST00000358671.9:c.646+248G>T
|
ENSP00000351497.5:n.646+248G>T
|
|
|
ENST00000367961.8:c.625+248G>T
|
ENSP00000356938.4:n.625+248G>T
|
|
|
ENST00000428605.3:c.646+248G>T
|
ENSP00000404329.3:n.646+248G>T
|
|
|
ENST00000480308.5:n.696+248G>T
|
|
|
|
ENST00000485778.1:n.2014+248G>T
|
|
|
|
NM_001002273.2:c.643+248G>T
|
NP_001002273.1:n.643+248G>T
|
|
|
NM_001002274.2:c.646+248G>T
|
NP_001002274.1:n.646+248G>T
|
|
|
NM_001002275.2:c.643+248G>T
|
NP_001002275.1:n.643+248G>T
|
|
|
NM_001190828.1:c.625+248G>T
|
NP_001177757.1:n.625+248G>T
|
|
|
NM_004001.4:c.646+248G>T
|
NP_003992.3:n.646+248G>T
|
|
|
XM_011509292.1:c.660G>T
|
XP_011507594.1:p.Arg220Ser
|
|
|
XM_017000670.2:c.643+248G>T
|
XP_016856159.1:n.643+248G>T
|
|
|
XM_024454043.1:c.646+248G>T
|
XP_024309811.1:n.646+248G>T
|
|
|
XM_024454044.1:c.643+248G>T
|
XP_024309812.1:n.643+248G>T
|
|
|
XM_024454045.1:c.643+248G>T
|
XP_024309813.1:n.643+248G>T
|
|
|
XM_024454047.1:c.660G>T
|
XP_024309815.1:p.Arg220Ser
|
|
|
NM_001002273.3:c.643+248G>T
|
NP_001002273.1:n.643+248G>T
|
|
|
NM_001002274.3:c.646+248G>T
|
NP_001002274.1:n.646+248G>T
|
|
|
NM_001002275.3:c.643+248G>T
|
NP_001002275.1:n.643+248G>T
|
|
|
NM_001190828.2:c.625+248G>T
|
NP_001177757.1:n.625+248G>T
|
|
|
NM_001386000.1:c.622+248G>T
|
NP_001372929.1:n.622+248G>T
|
|
|
NM_001386001.1:c.625+248G>T
|
NP_001372930.1:n.625+248G>T
|
|
|
NM_001386002.1:c.622+248G>T
|
NP_001372931.1:n.622+248G>T
|
|
|
NM_001386003.1:c.646+248G>T
|
NP_001372932.1:n.646+248G>T
|
|
|
NM_001386004.1:c.622+248G>T
|
NP_001372933.1:n.622+248G>T
|
|
|
NM_001386005.1:c.646+248G>T
|
NP_001372934.1:n.646+248G>T
|
|
|
NM_001386006.1:c.625+248G>T
|
NP_001372935.1:n.625+248G>T
|
|
|
NM_004001.5:c.646+248G>T
|
NP_003992.3:n.646+248G>T
|
|
|
NR_169827.1:n.875+248G>T
|
|
|
|
NM_001394477.1:c.646+248G>T
MANE Select
|
NP_001381406.1:n.646+248G>T
|
|
