ENST00000496887.7:c.1376-196G>T
|
ENSP00000434560.2:n.1376-196G>T
|
|
ENST00000646564.2:c.1193-196G>T
|
ENSP00000495806.2:n.1193-196G>T
|
|
ENST00000155840.12:c.1733-196G>T
MANE Select
|
ENSP00000155840.2:n.1733-196G>T
|
|
ENST00000335475.6:c.1352-196G>T
|
ENSP00000334497.5:n.1352-196G>T
|
|
ENST00000526095.2:c.103G>T
|
ENSP00000494939.1:p.Ala35Ser
|
|
ENST00000646564.1:c.839-196G>T
|
ENSP00000495806.1:n.839-196G>T
|
|
ENST00000155840.9:c.1733-196G>T
|
ENSP00000155840.2:n.1733-196G>T
|
|
ENST00000335475.5:c.1352-196G>T
|
ENSP00000334497.5:n.1352-196G>T
|
|
ENST00000526095.1:n.206G>T
|
|
|
NM_000218.2:c.1733-196G>T , LRG_287t1:c.1733-196G>T
|
NP_000209.2:n.1733-196G>T
|
|
NM_181798.1:c.1352-196G>T , LRG_287t2:c.1352-196G>T
|
NP_861463.1:n.1352-196G>T
|
|
NM_000218.3:c.1733-196G>T
MANE Select
|
NP_000209.2:n.1733-196G>T
|
|