ENST00000647956.2:c.1117+18G>A
MANE Select
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ENSP00000497341.1:n.1117+18G>A
|
|
ENST00000648162.1:n.1089+18G>A
|
|
|
ENST00000649804.1:c.211+18G>A
|
ENSP00000497938.1:n.211+18G>A
|
|
ENST00000535233.6:c.1015+18G>A
|
ENSP00000438636.3:n.1015+18G>A
|
|
ENST00000536053.6:c.1159+18G>A
|
ENSP00000444271.3:n.1159+18G>A
|
|
ENST00000540394.5:n.2182+18G>A
|
|
|
ENST00000542285.5:c.1117+18G>A
|
ENSP00000438615.2:n.1117+18G>A
|
|
ENST00000602298.2:n.1466+18G>A
|
|
|
NM_001733.4:c.1117+18G>A
|
NP_001724.3:n.1117+18G>A
|
|
NM_001354346.1:c.1159+18G>A
|
NP_001341275.1:n.1159+18G>A
|
|
NM_001733.6:c.1117+18G>A
|
NP_001724.4:n.1117+18G>A
|
|
NM_001733.7:c.1117+18G>A
MANE Select
|
NP_001724.4:n.1117+18G>A
|
|
NM_001354346.2:c.1159+18G>A
|
NP_001341275.1:n.1159+18G>A
|
|