ENST00000389048.8:c.3531G>A
MANE Select
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ENSP00000373700.3:p.Gln1177=
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|
ENST00000431873.6:c.758G>A
|
|
|
ENST00000638605.1:n.408G>A
|
|
|
ENST00000642122.1:c.327G>A
|
ENSP00000493203.1:p.Gln109=
|
|
ENST00000389048.7:c.3531G>A
|
ENSP00000373700.3:p.Gln1177=
|
|
ENST00000431873.5:c.411G>A
|
ENSP00000414027.2:p.Gln137=
|
|
ENST00000618119.4:c.2400G>A
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ENSP00000482733.1:p.Gln800=
|
|
NM_004304.4:c.3531G>A
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NP_004295.2:p.Gln1177=
|
|
NM_001353765.1:c.327G>A
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NP_001340694.1:p.Gln109=
|
|
XM_024452778.1:c.684G>A
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XP_024308546.1:p.Gln228=
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|
XM_024452779.1:c.327G>A
|
XP_024308547.1:p.Gln109=
|
|
NM_004304.5:c.3531G>A
MANE Select
|
NP_004295.2:p.Gln1177=
|
|
NM_001353765.2:c.327G>A
|
NP_001340694.1:p.Gln109=
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