ENST00000261609.13:c.11704G>A
MANE Select
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ENSP00000261609.8:p.Ala3902Thr
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ENST00000650509.1:c.3415G>A
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ENSP00000496936.1:p.Ala1139Thr
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ENST00000261609.11:c.11704G>A
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ENSP00000261609.7:p.Ala3902Thr
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ENST00000564519.1:n.219G>A
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|
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NM_004667.5:c.11704G>A
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NP_004658.3:p.Ala3902Thr
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XM_005268276.3:c.11590G>A
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XP_005268333.1:p.Ala3864Thr
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XM_005268277.3:c.11590G>A
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XP_005268334.1:p.Ala3864Thr
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XM_006720726.2:c.11689G>A
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XP_006720789.1:p.Ala3897Thr
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XM_006720727.2:c.11446G>A
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XP_006720790.1:p.Ala3816Thr
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XM_011522131.1:c.11221G>A
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XP_011520433.1:p.Ala3741Thr
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XM_011522132.1:c.9220G>A
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XP_011520434.1:p.Ala3074Thr
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XM_011522133.1:c.8449G>A
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XP_011520435.1:p.Ala2817Thr
|
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XM_011522134.1:c.5821G>A
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XP_011520436.1:p.Ala1941Thr
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XM_005268276.5:c.11590G>A
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XP_005268333.1:p.Ala3864Thr
|
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XM_006720726.3:c.11689G>A
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XP_006720789.1:p.Ala3897Thr
|
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XM_006720727.3:c.11446G>A
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XP_006720790.1:p.Ala3816Thr
|
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XM_017022695.1:c.11590G>A
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XP_016878184.1:p.Ala3864Thr
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XM_017022696.1:c.11590G>A
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XP_016878185.1:p.Ala3864Thr
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XM_017022697.1:c.4870G>A
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XP_016878186.1:p.Ala1624Thr
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|
XM_017022698.1:c.4870G>A
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XP_016878187.1:p.Ala1624Thr
|
|
NM_004667.6:c.11704G>A
MANE Select
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NP_004658.3:p.Ala3902Thr
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