ENST00000261609.13:c.11924T>G
MANE Select
|
ENSP00000261609.8:p.Val3975Gly
|
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ENST00000650509.1:c.3635T>G
|
ENSP00000496936.1:p.Val1212Gly
|
|
ENST00000261609.11:c.11924T>G
|
ENSP00000261609.7:p.Val3975Gly
|
|
NM_004667.5:c.11924T>G
|
NP_004658.3:p.Val3975Gly
|
|
XM_005268276.3:c.11810T>G
|
XP_005268333.1:p.Val3937Gly
|
|
XM_005268277.3:c.11810T>G
|
XP_005268334.1:p.Val3937Gly
|
|
XM_006720726.2:c.11909T>G
|
XP_006720789.1:p.Val3970Gly
|
|
XM_006720727.2:c.11666T>G
|
XP_006720790.1:p.Val3889Gly
|
|
XM_011522131.1:c.11441T>G
|
XP_011520433.1:p.Val3814Gly
|
|
XM_011522132.1:c.9440T>G
|
XP_011520434.1:p.Val3147Gly
|
|
XM_011522133.1:c.8669T>G
|
XP_011520435.1:p.Val2890Gly
|
|
XM_011522134.1:c.6041T>G
|
XP_011520436.1:p.Val2014Gly
|
|
XM_005268276.5:c.11810T>G
|
XP_005268333.1:p.Val3937Gly
|
|
XM_006720726.3:c.11909T>G
|
XP_006720789.1:p.Val3970Gly
|
|
XM_006720727.3:c.11666T>G
|
XP_006720790.1:p.Val3889Gly
|
|
XM_017022695.1:c.11810T>G
|
XP_016878184.1:p.Val3937Gly
|
|
XM_017022696.1:c.11810T>G
|
XP_016878185.1:p.Val3937Gly
|
|
XM_017022697.1:c.5090T>G
|
XP_016878186.1:p.Val1697Gly
|
|
XM_017022698.1:c.5090T>G
|
XP_016878187.1:p.Val1697Gly
|
|
NM_004667.6:c.11924T>G
MANE Select
|
NP_004658.3:p.Val3975Gly
|
|