ENST00000330498.4:c.1347C>A
MANE Select
|
ENSP00000327943.3:p.Gly449=
|
|
ENST00000330498.3:c.1347C>A
|
ENSP00000327943.3:p.Gly449=
|
|
ENST00000419665.6:c.1130-177C>A
|
ENSP00000410601.2:n.1130-177C>A
|
|
ENST00000568188.1:n.718C>A
|
|
|
ENST00000568891.1:n.282-177C>A
|
|
|
NM_003041.3:c.1347C>A
|
NP_003032.1:p.Gly449=
|
|
NR_130783.1:n.1149-177C>A
|
|
|
XM_006721072.2:c.1368C>A
|
XP_006721135.2:p.Gly456=
|
|
XM_006721073.2:c.1301+174C>A
|
XP_006721136.2:n.1301+174C>A
|
|
XM_006721072.4:c.1368C>A
|
XP_006721135.2:p.Gly456=
|
|
XM_024450402.1:c.1151-177C>A
|
XP_024306170.1:n.1151-177C>A
|
|
NM_003041.4:c.1347C>A
MANE Select
|
NP_003032.1:p.Gly449=
|
|
NR_130783.2:n.1144-177C>A
|
|
|