ENST00000255409.8:c.711+217G>C
MANE Select
|
ENSP00000255409.3:n.711+217G>C
|
|
ENST00000255409.7:c.711+217G>C
|
ENSP00000255409.3:n.711+217G>C
|
|
ENST00000404436.2:c.199+217G>C
|
|
|
ENST00000472064.1:n.235+217G>C
|
|
|
ENST00000473185.1:n.973+217G>C
|
|
|
NM_001276.2:c.711+217G>C
|
NP_001267.2:n.711+217G>C
|
|
XM_011509105.1:c.729+217G>C
|
XP_011507407.1:n.729+217G>C
|
|
XM_011509106.1:c.729+217G>C
|
XP_011507408.1:n.729+217G>C
|
|
XM_011509107.1:c.711+217G>C
|
XP_011507409.1:n.711+217G>C
|
|
XM_011509108.1:c.729+217G>C
|
XP_011507410.1:n.729+217G>C
|
|
NM_001276.3:c.711+217G>C
|
NP_001267.2:n.711+217G>C
|
|
NM_001276.4:c.711+217G>C
MANE Select
|
NP_001267.2:n.711+217G>C
|
|