ENST00000261609.13:c.11702T>G
MANE Select
|
ENSP00000261609.8:p.Val3901Gly
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ENST00000650509.1:c.3413T>G
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ENSP00000496936.1:p.Val1138Gly
|
|
ENST00000261609.11:c.11702T>G
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ENSP00000261609.7:p.Val3901Gly
|
|
ENST00000564519.1:n.217T>G
|
|
|
NM_004667.5:c.11702T>G
|
NP_004658.3:p.Val3901Gly
|
|
XM_005268276.3:c.11588T>G
|
XP_005268333.1:p.Val3863Gly
|
|
XM_005268277.3:c.11588T>G
|
XP_005268334.1:p.Val3863Gly
|
|
XM_006720726.2:c.11687T>G
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XP_006720789.1:p.Val3896Gly
|
|
XM_006720727.2:c.11444T>G
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XP_006720790.1:p.Val3815Gly
|
|
XM_011522131.1:c.11219T>G
|
XP_011520433.1:p.Val3740Gly
|
|
XM_011522132.1:c.9218T>G
|
XP_011520434.1:p.Val3073Gly
|
|
XM_011522133.1:c.8447T>G
|
XP_011520435.1:p.Val2816Gly
|
|
XM_011522134.1:c.5819T>G
|
XP_011520436.1:p.Val1940Gly
|
|
XM_005268276.5:c.11588T>G
|
XP_005268333.1:p.Val3863Gly
|
|
XM_006720726.3:c.11687T>G
|
XP_006720789.1:p.Val3896Gly
|
|
XM_006720727.3:c.11444T>G
|
XP_006720790.1:p.Val3815Gly
|
|
XM_017022695.1:c.11588T>G
|
XP_016878184.1:p.Val3863Gly
|
|
XM_017022696.1:c.11588T>G
|
XP_016878185.1:p.Val3863Gly
|
|
XM_017022697.1:c.4868T>G
|
XP_016878186.1:p.Val1623Gly
|
|
XM_017022698.1:c.4868T>G
|
XP_016878187.1:p.Val1623Gly
|
|
NM_004667.6:c.11702T>G
MANE Select
|
NP_004658.3:p.Val3901Gly
|
|