ENST00000319653.14:c.4859-14956T>C
MANE Select
|
ENSP00000318884.9:n.4859-14956T>C
|
|
ENST00000545751.3:c.700-14956T>C
|
|
|
ENST00000679390.1:n.1121-14956T>C
|
|
|
ENST00000679646.1:n.4325-14956T>C
|
|
|
ENST00000679980.1:c.1128-14956T>C
|
|
|
ENST00000681131.1:c.859-14956T>C
|
|
|
ENST00000681210.1:c.1079-14956T>C
|
ENSP00000505131.1:n.1079-14956T>C
|
|
ENST00000681296.1:n.2046-14956T>C
|
|
|
ENST00000681741.1:c.*903-14956T>C
|
ENSP00000505116.1:n.*903-14956T>C
|
|
ENST00000681805.1:c.744-14956T>C
|
|
|
ENST00000681824.1:c.986-14956T>C
|
ENSP00000505818.1:n.986-14956T>C
|
|
ENST00000319653.13:c.4859-14956T>C
|
ENSP00000318884.9:n.4859-14956T>C
|
|
ENST00000545751.2:c.287-14956T>C
|
ENSP00000437918.2:n.287-14956T>C
|
|
NM_001305424.1:c.4871-14956T>C
|
NP_001292353.1:n.4871-14956T>C
|
|
NM_020066.4:c.4859-14956T>C
|
NP_064450.3:n.4859-14956T>C
|
|
NM_001348094.1:c.2687-14956T>C
|
NP_001335023.1:n.2687-14956T>C
|
|
XM_017001840.2:c.2999-14956T>C
|
XP_016857329.1:n.2999-14956T>C
|
|
XM_017001841.2:c.2999-14956T>C
|
XP_016857330.1:n.2999-14956T>C
|
|
NM_020066.5:c.4859-14956T>C
MANE Select
|
NP_064450.3:n.4859-14956T>C
|
|
NM_001305424.2:c.4871-14956T>C
|
NP_001292353.1:n.4871-14956T>C
|
|
NM_001348094.2:c.2687-14956T>C
|
NP_001335023.1:n.2687-14956T>C
|
|