ENST00000225927.7:c.1765G>A
MANE Select
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ENSP00000225927.1:p.Ala589Thr
|
|
ENST00000225927.6:c.1765G>A
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ENSP00000225927.1:p.Ala589Thr
|
|
ENST00000591587.1:c.1103G>A
|
ENSP00000467836.1:n.1103G>A
|
|
NM_000263.3:c.1765G>A
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NP_000254.2:p.Ala589Thr
|
|
XM_006721920.2:c.934G>A
|
XP_006721983.1:p.Ala312Thr
|
|
XM_011524840.1:c.766G>A
|
XP_011523142.1:p.Ala256Thr
|
|
XM_017024687.1:c.934G>A
|
XP_016880176.1:p.Ala312Thr
|
|
XM_024450771.1:c.1822G>A
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XP_024306539.1:p.Ala608Thr
|
|
XM_024450772.1:c.766G>A
|
XP_024306540.1:p.Ala256Thr
|
|
NM_000263.4:c.1765G>A
MANE Select
|
NP_000254.2:p.Ala589Thr
|
|