ENST00000683572.1:n.697C>G
|
|
|
ENST00000341947.7:c.4891C>G
MANE Select
|
ENSP00000339915.2:p.Pro1631Ala
|
|
ENST00000341947.6:c.4891C>G
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ENSP00000339915.2:p.Pro1631Ala
|
|
ENST00000361917.5:c.4570C>G
|
ENSP00000355123.1:p.Pro1524Ala
|
|
ENST00000374708.8:c.4633C>G
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ENSP00000363840.4:p.Pro1545Ala
|
|
ENST00000477772.1:n.681C>G
|
|
|
NM_080679.2:c.4570C>G
|
NP_542410.2:p.Pro1524Ala
|
|
NM_080680.2:c.4891C>G
|
NP_542411.2:p.Pro1631Ala
|
|
NM_080681.2:c.4633C>G
|
NP_542412.2:p.Pro1545Ala
|
|
XM_011514298.1:c.4045C>G
|
XP_011512600.1:p.Pro1349Ala
|
|
XM_011514299.1:c.4177C>G
|
XP_011512601.1:p.Pro1393Ala
|
|
XM_011514300.1:c.3997C>G
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XP_011512602.1:p.Pro1333Ala
|
|
XM_011514301.1:c.3934C>G
|
XP_011512603.1:p.Pro1312Ala
|
|
XM_011514302.1:c.3778C>G
|
XP_011512604.1:p.Pro1260Ala
|
|
XM_011514299.2:c.4177C>G
|
XP_011512601.1:p.Pro1393Ala
|
|
XM_011514300.2:c.3997C>G
|
XP_011512602.1:p.Pro1333Ala
|
|
XM_011514302.2:c.3778C>G
|
XP_011512604.1:p.Pro1260Ala
|
|
XM_017010250.1:c.4891C>G
|
XP_016865739.1:p.Pro1631Ala
|
|
XM_017010251.2:c.3709C>G
|
XP_016865740.1:p.Pro1237Ala
|
|
NM_080680.3:c.4891C>G
MANE Select
|
NP_542411.2:p.Pro1631Ala
|
|
NM_080681.3:c.4633C>G
|
NP_542412.2:p.Pro1545Ala
|
|
NM_080679.3:c.4570C>G
|
NP_542410.2:p.Pro1524Ala
|
|