ENST00000572933.6:c.399+2714A>C
MANE Select
|
ENSP00000458355.1:n.399+2714A>C
|
|
ENST00000389173.6:c.399+2714A>C
|
ENSP00000373825.2:n.399+2714A>C
|
|
ENST00000570791.5:c.399+2714A>C
|
ENSP00000460245.1:n.399+2714A>C
|
|
ENST00000572933.5:c.399+2714A>C
|
ENSP00000458355.1:n.399+2714A>C
|
|
NM_001303270.1:c.399+2714A>C
|
NP_001290199.1:n.399+2714A>C
|
|
NM_020877.3:c.399+2714A>C
|
NP_065928.2:n.399+2714A>C
|
|
XM_011523663.1:c.399+2714A>C
|
XP_011521965.1:n.399+2714A>C
|
|
XM_011523664.1:c.399+2714A>C
|
XP_011521966.1:n.399+2714A>C
|
|
XM_011523665.1:c.399+2714A>C
|
XP_011521967.1:n.399+2714A>C
|
|
XM_011523666.1:c.399+2714A>C
|
XP_011521968.1:n.399+2714A>C
|
|
XM_011523667.1:c.399+2714A>C
|
XP_011521969.1:n.399+2714A>C
|
|
XM_011523670.1:c.399+2714A>C
|
XP_011521972.1:n.399+2714A>C
|
|
XM_011523667.2:c.399+2714A>C
|
XP_011521969.1:n.399+2714A>C
|
|
XM_011523670.2:c.399+2714A>C
|
XP_011521972.1:n.399+2714A>C
|
|
XM_017024219.1:c.399+2714A>C
|
XP_016879708.1:n.399+2714A>C
|
|
XM_024450604.1:c.399+2714A>C
|
XP_024306372.1:n.399+2714A>C
|
|
XM_024450605.1:c.399+2714A>C
|
XP_024306373.1:n.399+2714A>C
|
|
XM_024450606.1:c.399+2714A>C
|
XP_024306374.1:n.399+2714A>C
|
|
XM_024450607.1:c.399+2714A>C
|
XP_024306375.1:n.399+2714A>C
|
|
NM_001303270.2:c.399+2714A>C
|
NP_001290199.1:n.399+2714A>C
|
|
NM_020877.4:c.399+2714A>C
|
NP_065928.2:n.399+2714A>C
|
|
NM_020877.5:c.399+2714A>C
MANE Select
|
NP_065928.2:n.399+2714A>C
|
|