ENST00000248846.10:c.2151G>T
MANE Select
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ENSP00000248846.5:p.Gln717His
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ENST00000248846.9:c.2151G>T
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ENSP00000248846.5:p.Gln717His
|
|
ENST00000439308.6:c.2151G>T
|
ENSP00000397387.2:p.Gln717His
|
|
ENST00000473946.1:n.460G>T
|
|
|
ENST00000489511.5:n.168G>T
|
|
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ENST00000491449.5:n.458G>T
|
|
|
ENST00000498611.5:n.2684G>T
|
|
|
NM_020461.3:c.2151G>T
|
NP_065194.2:p.Gln717His
|
|
XR_938347.1:n.2716G>T
|
|
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XR_938348.1:n.2716G>T
|
|
|
XR_001755343.2:n.2720G>T
|
|
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XR_001755344.2:n.2720G>T
|
|
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XR_002958720.1:n.2720G>T
|
|
|
XR_938347.2:n.2720G>T
|
|
|
NM_020461.4:c.2151G>T
MANE Select
|
NP_065194.3:p.Gln717His
|
|