ENST00000261609.13:c.11975G>T
MANE Select
|
ENSP00000261609.8:p.Gly3992Val
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ENST00000650509.1:c.3686G>T
|
ENSP00000496936.1:p.Gly1229Val
|
|
ENST00000261609.11:c.11975G>T
|
ENSP00000261609.7:p.Gly3992Val
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NM_004667.5:c.11975G>T
|
NP_004658.3:p.Gly3992Val
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XM_005268276.3:c.11861G>T
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XP_005268333.1:p.Gly3954Val
|
|
XM_005268277.3:c.11861G>T
|
XP_005268334.1:p.Gly3954Val
|
|
XM_006720726.2:c.11960G>T
|
XP_006720789.1:p.Gly3987Val
|
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XM_006720727.2:c.11717G>T
|
XP_006720790.1:p.Gly3906Val
|
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XM_011522131.1:c.11492G>T
|
XP_011520433.1:p.Gly3831Val
|
|
XM_011522132.1:c.9491G>T
|
XP_011520434.1:p.Gly3164Val
|
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XM_011522133.1:c.8720G>T
|
XP_011520435.1:p.Gly2907Val
|
|
XM_011522134.1:c.6092G>T
|
XP_011520436.1:p.Gly2031Val
|
|
XM_005268276.5:c.11861G>T
|
XP_005268333.1:p.Gly3954Val
|
|
XM_006720726.3:c.11960G>T
|
XP_006720789.1:p.Gly3987Val
|
|
XM_006720727.3:c.11717G>T
|
XP_006720790.1:p.Gly3906Val
|
|
XM_017022695.1:c.11861G>T
|
XP_016878184.1:p.Gly3954Val
|
|
XM_017022696.1:c.11861G>T
|
XP_016878185.1:p.Gly3954Val
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XM_017022697.1:c.5141G>T
|
XP_016878186.1:p.Gly1714Val
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XM_017022698.1:c.5141G>T
|
XP_016878187.1:p.Gly1714Val
|
|
NM_004667.6:c.11975G>T
MANE Select
|
NP_004658.3:p.Gly3992Val
|
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