ENST00000696170.1:c.*15T>G
|
ENSP00000512461.1:n.*15T>G
|
|
ENST00000696171.1:c.410T>G
|
ENSP00000512462.1:p.Leu137Arg
|
|
ENST00000696172.1:c.338-2982T>G
|
ENSP00000512463.1:n.338-2982T>G
|
|
ENST00000378588.5:c.506T>G
MANE Select
|
ENSP00000367851.4:p.Leu169Arg
|
|
ENST00000378588.4:c.506T>G
|
ENSP00000367851.4:p.Leu169Arg
|
|
ENST00000465127.1:c.171+369973T>G
|
ENSP00000417050.1:n.171+369973T>G
|
|
NM_000397.3:c.506T>G , LRG_53t1:c.506T>G
|
NP_000388.2:p.Leu169Arg
|
|
XM_011543890.1:c.200T>G
|
XP_011542192.1:p.Leu67Arg
|
|
NM_000397.4:c.506T>G
MANE Select
|
NP_000388.2:p.Leu169Arg
|
|