ENST00000264595.7:c.414T>G
MANE Select
|
ENSP00000264595.2:p.Ser138Arg
|
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ENST00000264595.6:c.414T>G
|
ENSP00000264595.2:p.Ser138Arg
|
|
ENST00000502310.5:c.69T>G
|
ENSP00000423798.1:p.Ser23Arg
|
|
ENST00000506853.5:n.448T>G
|
|
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ENST00000510635.1:c.110T>G
|
|
|
ENST00000510955.5:n.335T>G
|
|
|
NM_000027.3:c.414T>G
|
NP_000018.2:p.Ser138Arg
|
|
NM_001171988.1:c.414T>G
|
NP_001165459.1:p.Ser138Arg
|
|
NR_033655.1:n.542T>G
|
|
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XM_006714123.2:c.414T>G
|
XP_006714186.1:p.Ser138Arg
|
|
XR_001741155.2:n.508T>G
|
|
|
NM_000027.4:c.414T>G
MANE Select
|
NP_000018.2:p.Ser138Arg
|
|
NM_001171988.2:c.414T>G
|
NP_001165459.1:p.Ser138Arg
|
|
NR_033655.2:n.476T>G
|
|
|