ENST00000338508.9:c.3375A>G
|
ENSP00000345193.7:p.Pro1125=
|
|
ENST00000412252.6:c.920A>G
|
ENSP00000414876.2:n.920A>G
|
|
ENST00000601538.6:c.5142A>G
MANE Select
|
ENSP00000469689.2:p.Pro1714=
|
|
ENST00000654939.1:c.2651A>G
|
|
|
ENST00000656230.1:c.4005A>G
|
ENSP00000499561.1:p.Pro1335=
|
|
ENST00000659264.1:c.3432A>G
|
ENSP00000499270.1:p.Pro1144=
|
|
ENST00000338508.8:c.3378A>G
|
ENSP00000345193.6:p.Pro1126=
|
|
ENST00000357171.7:c.*146A>G
|
ENSP00000349694.4:n.*146A>G
|
|
ENST00000409161.5:c.3354A>G
|
ENSP00000386491.1:p.Pro1118=
|
|
ENST00000412252.5:c.918A>G
|
|
|
ENST00000423696.6:c.4005A>G
|
ENSP00000394536.2:p.Pro1335=
|
|
ENST00000424924.5:c.2979A>G
|
ENSP00000402944.1:p.Pro993=
|
|
ENST00000449833.6:c.3378A>G
|
ENSP00000399423.3:p.Pro1126=
|
|
ENST00000601538.5:c.5142A>G
|
ENSP00000469689.2:p.Pro1714=
|
|
ENST00000606715.3:n.1894A>G
|
|
|
NM_012309.4:c.5142A>G
|
NP_036441.2:p.Pro1714=
|
|
NM_133266.4:c.3378A>G
|
NP_573573.2:p.Pro1126=
|
|
NR_110766.1:n.996A>G
|
|
|
XM_005277930.2:c.5142A>G
|
XP_005277987.1:p.Pro1714=
|
|
XM_005277932.2:c.4005A>G
|
XP_005277989.1:p.Pro1335=
|
|
XM_006718478.2:c.5112A>G
|
XP_006718541.1:p.Pro1704=
|
|
XM_011544854.1:c.5154A>G
|
XP_011543156.1:p.Pro1718=
|
|
XM_011544855.1:c.5133A>G
|
XP_011543157.1:p.Pro1711=
|
|
XM_011544856.1:c.5127A>G
|
XP_011543158.1:p.Pro1709=
|
|
XM_011544857.1:c.5106A>G
|
XP_011543159.1:p.Pro1702=
|
|
XM_011544859.1:c.4017A>G
|
XP_011543161.1:p.Pro1339=
|
|
XM_005277932.3:c.4005A>G
|
XP_005277989.1:p.Pro1335=
|
|
XM_017017387.1:c.5142A>G
|
XP_016872876.1:p.Pro1714=
|
|
XM_017017388.1:c.5142A>G
|
XP_016872877.1:p.Pro1714=
|
|
XM_017017389.1:c.5115A>G
|
XP_016872878.1:p.Pro1705=
|
|
XM_017017390.1:c.3432A>G
|
XP_016872879.1:p.Pro1144=
|
|
NM_133266.5:c.3378A>G
|
NP_573573.2:p.Pro1126=
|
|
NR_110766.2:n.997A>G
|
|
|
NM_001379226.1:c.4005A>G
|
NP_001366155.1:p.Pro1335=
|
|
NM_012309.5:c.5142A>G
MANE Select
|
NP_036441.2:p.Pro1714=
|
|