ENST00000294304.12:c.3913T>G
MANE Select
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ENSP00000294304.6:p.Cys1305Gly
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ENST00000294304.11:c.3913T>G
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ENSP00000294304.6:p.Cys1305Gly
|
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ENST00000529993.5:c.*2519T>G
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ENSP00000436652.1:n.*2519T>G
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NM_001291902.1:c.2170T>G
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NP_001278831.1:p.Cys724Gly
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NM_002335.3:c.3913T>G
|
NP_002326.2:p.Cys1305Gly
|
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XM_005273994.2:c.3913T>G
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XP_005274051.1:p.Cys1305Gly
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XM_011545029.1:c.3940T>G
|
XP_011543331.1:p.Cys1314Gly
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XM_011545030.1:c.3940T>G
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XP_011543332.1:p.Cys1314Gly
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XM_011545031.1:c.3940T>G
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XP_011543333.1:p.Cys1314Gly
|
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XR_949925.1:n.3955T>G
|
|
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XR_949926.1:n.3955T>G
|
|
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XM_017017735.1:c.2170T>G
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XP_016873224.1:p.Cys724Gly
|
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XM_017017736.1:c.1453T>G
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XP_016873225.1:p.Cys485Gly
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XR_949925.2:n.3955T>G
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|
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XR_949926.2:n.3955T>G
|
|
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NM_002335.4:c.3913T>G
MANE Select
|
NP_002326.2:p.Cys1305Gly
|
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NM_001291902.2:c.2170T>G
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NP_001278831.1:p.Cys724Gly
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