ENST00000367649.8:c.202+78379G>C
MANE Select
|
ENSP00000356621.3:n.202+78379G>C
|
|
ENST00000367649.7:c.202+78379G>C
|
ENSP00000356621.3:n.202+78379G>C
|
|
ENST00000465723.1:n.526+47572G>C
|
|
|
NM_170692.2:c.202+78379G>C
|
NP_733793.2:n.202+78379G>C
|
|
XM_011510166.1:c.202+78379G>C
|
XP_011508468.1:n.202+78379G>C
|
|
XM_011510167.1:c.202+78379G>C
|
XP_011508469.1:n.202+78379G>C
|
|
XM_011510168.1:c.202+78379G>C
|
XP_011508470.1:n.202+78379G>C
|
|
XM_011510166.2:c.202+78379G>C
|
XP_011508468.1:n.202+78379G>C
|
|
XM_011510167.2:c.202+78379G>C
|
XP_011508469.1:n.202+78379G>C
|
|
NM_170692.4:c.202+78379G>C
MANE Select
|
NP_733793.2:n.202+78379G>C
|
|