ENST00000248846.10:c.3895G>C
MANE Select
|
ENSP00000248846.5:p.Gly1299Arg
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ENST00000248846.9:c.3895G>C
|
ENSP00000248846.5:p.Gly1299Arg
|
|
ENST00000439308.6:c.3895G>C
|
ENSP00000397387.2:p.Gly1299Arg
|
|
ENST00000491449.5:n.2202G>C
|
|
|
ENST00000498611.5:n.3618-449G>C
|
|
|
NM_020461.3:c.3895G>C
|
NP_065194.2:p.Gly1299Arg
|
|
XR_938347.1:n.4460G>C
|
|
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XR_938348.1:n.3050-449G>C
|
|
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XR_001755343.2:n.4464G>C
|
|
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XR_001755344.2:n.4464G>C
|
|
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XR_002958720.1:n.3054-449G>C
|
|
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XR_938347.2:n.4464G>C
|
|
|
NM_020461.4:c.3895G>C
MANE Select
|
NP_065194.3:p.Gly1299Arg
|
|